Label: AMMONIA INHALANTS inhalant
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Contains inactivated NDC Code(s)
NDC Code(s): 70385-2003-3 - Packager: Sina Health Inc
- This is a repackaged label.
- Source NDC Code(s): 39822-9900
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 4, 2019
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INGREDIENTS AND APPEARANCE
AMMONIA INHALANTS
ammonia inhalants inhalantProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70385-2003(NDC:39822-9900) Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 0.045 g in 0.3 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) FD&C RED NO. 40 (UNII: WZB9127XOA) LAVENDER OIL (UNII: ZBP1YXW0H8) WATER (UNII: 059QF0KO0R) NUTMEG OIL (UNII: Z1CLM48948) LEMON OIL (UNII: I9GRO824LL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70385-2003-3 3 in 1 BAG 04/18/2016 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 - Sina Health Inc (047161553) Registrant - Sina Health Inc (047191553) Establishment Name Address ID/FEI Business Operations Sina Health Inc 047161553 repack(70385-2003)