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Analpram HC

hydrocortisone acetate and pramoxine hydrochloride · Lotion

Prescription ANDA Official labelling
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Analpram HC
Generic name
hydrocortisone acetate and pramoxine hydrochloride
Dosage form
Lotion
Route
Topical
Marketing category
ANDA · ANDA
Labeler
Sebela Pharmaceuticals Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
2
NDC product codes
2
Packages
2
Data completeness
76% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Hydrocortisone Acetate 25 mg/mL 1291082 View
Pramoxine Hydrochloride 10 mg/mL 1234532 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Lotion
Route of administration
Topical
Presentations
4

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Corticosteroid Hormone Receptor Agonists [MoA] MoA All 215 members
Corticosteroid [EPC] EPC All 215 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
085979
Application type
ANDA · Abbreviated New Drug Application
Approval date
June 5, 1978
Sponsor
LEGACY
Products on application
1
Submissions recorded
9
Products approved under application 085979.
Product Trade name Form Strength Ingredient Status TE Flags
085979-001 PRAMOSONE LOTION HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE Prescription —

Approval history

Source: Drugs@FDA
Most recent submissions on application 085979.
Type No. Action Status Date Review
Supplement 14 Manufacturing (CMC) Approved January 24, 2002 —
Supplement 15 Manufacturing (CMC) Approved November 21, 2001 —
Supplement 13 Manufacturing (CMC) Approved June 9, 2000 —
Supplement 12 Manufacturing (CMC) Approved March 1, 1999 —
Supplement 10 Manufacturing (CMC) Approved October 14, 1992 —
Supplement 9 Labeling Approved October 14, 1992 —
Supplement 8 Manufacturing (CMC) Approved October 14, 1992 —
Supplement 11 Manufacturing (CMC) Approved August 20, 1992 —
Original application 1 Approved June 5, 1978 —

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20251108). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20251108 HUMAN PRESCRIPTION DRUG · 20250609

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE: Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION: Topical corticosteroids are generally applied to the affected area as a thin film three to four times daily depending on the severity of the condition. Lotion should be shaken well before use. Occlusive dressings may be used for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted. For cleansing the anogenital area, apply with a tissue or cotton ball.

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS: Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS: The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: Burning Hypertrichosis Maceration of the skin Itching Acneiform eruptions Secondary infection Irritation Hypopigmentation Skin atrophy Dryness Perioral dermatitis Striae Folliculitis Allergic contact dermatitis Miliaria

Description

openFDA Drug Labeling

DESCRIPTION: Analpram HC ® Lotion 2.5% is a topical preparation containing hydrocortisone acetate 2.5% w/w and pramoxine hydrochloride 1% w/w in a hydrophilic lotion base containing stearic acid, cetyl alcohol, FORLAN-L (Contains: petrolatum, lanolin, hydrogenated coconut oil, sorbitan sesquioleate, stearyl alcohol, and cetyl alcohol), glycerin, trolamine, polyoxyl 40 stearate, di-isopropyl adipate, povidone, dimethicone, potassium sorbate, sorbic acid, and purified water. Topical corticosteroids are anti-inflammatory and anti-pruritic agents. The structural formula, the chemical name, molecular formula and molecular weight for active ingredients are presented as follows: hydrocortisone acetate Pregn-4-ene-3, 20-dione, 21-(acetyloxy)-11, 17-dihydroxy-, (11-beta)- C 23 H 32 O 6 ; mol. wt.: 404.50 pramoxine hydrochloride 4-(3-(p-butoxyphenoxy)propyl)morpholine hydrochloride C 17 H 27 NO 3 .HCl ; mol. wt.: 329.87 hydrocortisone acetate pramoxine hydrochloride

OVERDOSAGE: Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects. (See PRECAUTIONS. )

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED: Analpram HC ® Lotion 2.5% 2 fl oz (NDC 54766-829-04) Storage Conditions: Store at 25°C (77°F); excursions permitted to 15-30°C (59-85°F) [see USP Controlled Room Temperature]. Rx Only Manufactured for Sebela Ireland Ltd. By Ferndale Laboratories, Inc., Ferndale, MI 48220 U.S.A. Distributed by Sebela Pharmaceuticals Inc. 645 Hembree Parkway, Suite I Roswell, GA 30076 www.sebelapharma.com Toll Free 1-844-732-3521 PI 829040215 Rev. Feb. 2015 Analpram HC ® is a registered trademark of Sebela International Limited. ©2015 Reproduction prohibited

Adverse event reports

Source: openFDA FAERS
73,232
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: HYDROCORTISONE ACETATE. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
83107-020-02 83107-020 Legacy Pharma USA Inc. 59 mL in 1 BOTTLE, PLASTIC (83107-020-02) May 23, 2025
54766-829-04 54766-829 Sebela Pharmaceuticals Inc. 59 mL in 1 BOTTLE, PLASTIC (54766-829-04) August 5, 2015
83107-020 83107-020 Legacy Pharma USA Inc. — May 23, 2025
54766-829 54766-829 Sebela Pharmaceuticals Inc. — August 5, 2015

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
Drug Labeling FDA / NLM Prescribing information reproduced above
FAERS FDA Adverse event report counts

Generated September 25, 2026 · 11 sections on this page.