Label: AMMONIA INHALANTS inhalant
- NDC Code(s): 67777-251-01, 67777-251-02
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 28, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- Label
-
INGREDIENTS AND APPEARANCE
AMMONIA INHALANTS
ammonia inhalants inhalantProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-251 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 0.05 g in 0.33 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-251-02 500 in 1 CASE 02/14/1976 1 NDC:67777-251-01 10 in 1 BOX 1 0.33 mL in 1 AMPULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/14/1976 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124529)