Label: ZEROSWEAT 3 DAY PROTECTION ANTIPERSPIRANT- aluminum chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 55726-048-01 - Packager: ZeroSweat Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 15, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL - 35.5 ml Bottle Carton
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INGREDIENTS AND APPEARANCE
ZEROSWEAT 3 DAY PROTECTION ANTIPERSPIRANT
aluminum chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55726-048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55726-048-01 35.5 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/11/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 06/11/2012 Labeler - ZeroSweat Inc (078507610) Registrant - Solo Laboratories, Inc. (005126784) Establishment Name Address ID/FEI Business Operations BMC1092 dba Solo Laboratories , Inc 078831987 manufacture(55726-048)