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Helium

Active ingredient 7 prescription 2 over-the-counter 1 with labelling

Overview

Source: NDC Directory
Ingredient name
HELIUM
Base moiety
HELIUM
RxNorm CUI
UNII
206GF3GB41
Medication products
9
Brand names
9
Dosage forms
2
FAERS reports
48,982 · not a risk measure

Products containing this ingredient

Source: NDC Directory 9 products
  • COMPRESSED Gas OXIDIZING, N.O.S. OXYGEN, Helium · Gas
    Rx 1 NDC
  • COMPRESSED Gas, N.O.S. OXYGEN, Helium · Gas
    Rx 2 NDC
  • Gut Brain Spectrum Abrotanum (Artemisia Abrotanum), Aethusa Cynapium, Baptisia Tinctoria, Cicuta Virosa, Cuprum Metallicum, Mezereum, Bufo Rana, Lac Materna Humanum, Saccharum Officinale, Serotonin (Hydrochloride), Alumina, Calcarea Phosphorica, Candida Albicans, Carcinosin, Lac Caninum, Mercurius Solubilis, Natrum Muriaticum, Propionic Acid, Sulphur, Thuja Occidentalis, Formalinum, Morbillinum · Liquid
    OTC 2 NDC
  • Helium Oxygen Nitrogen mixture Gas
    Rx 1 NDC
  • Spectric Agaricus Muscarius, Aspartame, Bufo Rana, Carcinosin, Cerebrum Suis, Ethylicum, Helleborus Niger, Hydrogen, Hyoscyamus Niger, Kali Bromatum, L-Dopa, Neon, Olibanum (Boswellia Serrata), Placenta Totalis Suis, Serotonin (Hydrochloride), Stramonium, Thuja Occidentalis · Liquid
    OTC 3 NDC
  • Helium Gas
    Rx NDA 16 NDC
  • Helium Oxygen mixture Gas
    Rx NDA 2 NDC
  • Helium, Oxygen Gas
    Rx NDA 2 NDC
  • XENOVIEW xenon Xe 129 hyperpolarized · Gas
    Rx NDA 5 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form Products Examples
Gas 7 COMPRESSED Gas OXIDIZING, N.O.S., COMPRESSED Gas, N.O.S., Helium Oxygen Nitrogen mixture, Helium …
Liquid 2 Gut Brain Spectrum, Spectric

Sources for this page

Dataset Agency Used for
NDC Directory FDA Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings NLM RxNorm concept identifier (RxCUI)
FAERS FDA Adverse event report totals