Label: AXE- acne control body hand and face bar soap
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-2025-1 - Packager: Conopco Inc. d/b/a/ Unilever
- 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 April 29, 2022
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- Official Label (Printer Friendly)
- AXE ACNE CONTROL BODY, HAND AND FACE BAR - Salicylic Acid
- Drug Facts
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive ingredients
Sodium Palmate, Sodium Palm Kernelate, Water (Aqua), Glycerin, Sodium Gluconate, Fragrance (Parfum), Palm Acid, Sodium Chloride, Palm Kernel Acid, Petroselinum Sativum (Parsley) Leaf Powder, Curcuma Longa (Tumeric) Root Extract, Melaleuca Alternifolia (Ta Tree) Flower/Leaf/Stem Extract, Titanium Dioxide (CI 77891), Ext. Yellow 7 (CI 42053), Iron Oxides (CI 77499).
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- Packaging
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INGREDIENTS AND APPEARANCE
AXE
acne control body hand and face bar soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-2025 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 EXT. D&C YELLOW NO. 7 (UNII: 08F8S9O3I5) SODIUM PALMATE (UNII: S0A6004K3Z) SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) GLYCERIN (UNII: PDC6A3C0OX) SODIUM GLUCONATE (UNII: R6Q3791S76) PALM ACID (UNII: B6G0Y5Z616) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PALM KERNEL ACID (UNII: 79P21R4317) PARSLEY (UNII: 58FMD0Q0EV) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) FERRIC OXIDE RED (UNII: 1K09F3G675) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-2025-1 127.5 g in 1 CARTON; Type 0: Not a Combination Product 04/29/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 04/29/2022 Labeler - Conopco Inc. d/b/a/ Unilever (001375088)