Label: ZEROSWEAT ANTIPERSPIRANT 12%- antiperspirant lotion
- NDC Code(s): 65112-306-01, 65112-306-02
- Packager: I. Shay Cosmetics
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
-
WARNINGS
For External Use Only.
Ask a doctor before use if you have kidney disease.
Do not use:
-Immediately after shaving
-On irritated skin
-On broken skin
-Immediately after bathing
When using this product do not use in or near eyes.
Stop use and ask doctor if rash or irritation develops
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ZEROSWEAT ANTIPERSPIRANT 12%
antiperspirant lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65112-306 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 35.5 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65112-306-02 1 in 1 BOX 06/01/2024 1 NDC:65112-306-01 35.5 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 06/01/2024 Labeler - I. Shay Cosmetics (151582384)