AXE- acne control body hand and face bar soap

Axe by

Drug Labeling and Warnings

Axe by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AXE ACNE CONTROL BODY, HAND AND FACE BAR - Salicylic Acid

Dove Care & Protect Antibacterial Beauty Bar

Drug Facts

Active ingredient

Salicylic Acid (2.0)

Purpose

Acne Treatment

Uses

For the treatment of acne

Warnings

For external use only
When using this product, skin irritation and dryness is more likely to occur if you use anoter tropical acne medication at the same time. If irritation occurs, only use one tropical acne medication at a time.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children except under adult supervision.

If swallowed, get medical help or contact a poison control Center right away.

Directions

Lather on body and face. Rinse. Feel great.

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).

Question/Comments?

1-800-450-7580

Packaging

INGREDIENTS AND APPEARANCE

AXE 
acne control body hand and face bar soap

Product 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 Drug	M006	04/29/2022

Labeler - Conopco Inc. d/b/a/ Unilever (001375088)