Label: AXE ACNE CONTROL 2% SALICYLIC ACID- salicylic acid 2% soap
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-3785-8 - Packager: CONOPCO, INC. D/B/A/ UNILEVER
- 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 November 24, 2020
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Use
- Warnings
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive Ingredients
Inactive ingredients
Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Gluconate, Fragrance (Natural), Palm Acid, Sodium Chloride, Palm Kernel Acid, Petroselinum Sativum (Parsley) Leaf Powder, Titanium Dioxide (CI 77891), Ext. Yellow 7 (CI 10316), Iron Oxides (CI 77499), Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract,
Curcuma Longa (Turmeric) Root Extract, Green 3 (CI 42053) - SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AXE ACNE CONTROL 2% SALICYLIC ACID
salicylic acid 2% soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-3785 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Inactive Ingredients Ingredient Name Strength FERROSOFERRIC OXIDE (UNII: XM0M87F357) TURMERIC (UNII: 856YO1Z64F) EXT. D&C YELLOW NO. 7 (UNII: 08F8S9O3I5) SODIUM CHLORIDE (UNII: 451W47IQ8X) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) SODIUM GLUCONATE (UNII: R6Q3791S76) PARSLEY (UNII: 58FMD0Q0EV) GLYCERIN (UNII: PDC6A3C0OX) SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) PALM ACID (UNII: B6G0Y5Z616) SODIUM PALMATE (UNII: S0A6004K3Z) PALM KERNEL ACID (UNII: 79P21R4317) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-3785-8 127.5 g in 1 CARTON; Type 0: Not a Combination Product 11/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/24/2020 Labeler - CONOPCO, INC. D/B/A/ UNILEVER (001375088)