Label: AMMONIA PAD- ammonia inhalant
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Contains inactivated NDC Code(s)
NDC Code(s): 52124-3201-1, 52124-3201-2 - Packager: Genuine First Aid, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 4, 2011
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- Official Label (Printer Friendly)
- Content
- Purpose
- Uses
- Caution
- Inactive Ingredients
- Directions
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AMMONIA PAD
ammonia inhalantProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52124-3201 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 10 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-3201-1 0.5 mL in 1 PACKET 2 NDC:52124-3201-2 100 in 1 BOX 2 0.5 mL in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/04/2011 Labeler - Genuine First Aid, LLC (619609857)