Label: ZEROSWEAT WITH ALOE- antiperspirant liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 65112-259-01 - Packager: I Shay Cosmetics Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 June 28, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
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WARNINGS
For external use only.
Do not use:
- Immediately after shaving
- Immediately after bathing
- On irritated skin
- On broken skin
Stop use if rash occurs
Ask a doctor before use if you have kidney diseaseKeep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZEROSWEAT WITH ALOE
antiperspirant liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65112-259 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE 0.12 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.85 g in 1 g ALLANTOIN (UNII: 344S277G0Z) 0.005 g in 1 g GLYCERIN (UNII: PDC6A3C0OX) 0.02 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65112-259-01 28.35 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 03/14/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 03/14/2019 Labeler - I Shay Cosmetics Inc (151582384)