Label: OVERNIGHT SPOT TREATMENT- acne treatment liquid
- NDC Code(s): 70060-1506-1
- Packager: CosMedical Technologies
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 10, 2023
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- Official Label (Printer Friendly)
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
OVERNIGHT SPOT TREATMENT
acne treatment liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70060-1506 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) ZINC OXIDE (UNII: SOI2LOH54Z) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70060-1506-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/04/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 11/04/2015 Labeler - CosMedical Technologies (803898329) Registrant - CosMedical Technologies (803898329)
