FDA.reportPublic FDA data

AXE Acne Control 2% Salicylic Acid

Manufacturer
CONOPCO, INC. D/B/A/ UNILEVER
Effective date
2020-11-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:05:38

Label at a glance#

ProductAXE Acne Control 2% Salicylic Acid
Active ingredientSALICYLIC ACID
Label structure11 sections

Dosage and administration

Directions Lather on body and face. Rinse. Feel great.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic acid 2%

OTC - PURPOSE SECTION

Purpose

Acne treatment

Use

INDICATIONS & USAGE SECTION

Uses

  • For the treatment of acne

Warnings

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product, skin irritation and dryness may occur if you use other topical acne medications at the same time. If irritation occurs, use only one medication at a time.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • Lather on body and face. Rinse. Feel great.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Distributed by:

UNILEVER, TRUMBULL, CT 06611

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AXE ACNE CONTROL

2% Salicylic Acid

CartonCarton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-3785-82024-10-23C16284748780-1d6a99b39-e70e-a426-e053-dadaa90af4c2AXE Acne Control
64942-3785-82022-01-28C16284748780-1d6a99b39-e70e-a426-e053-dadaa90af4c2AXE Acne Control

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-378564942-3785-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
FERROSOFERRIC OXIDEXM0M87F357IACT
TURMERIC856YO1Z64FIACT
EXT. D&C YELLOW NO. 708F8S9O3I5IACT
SODIUM CHLORIDE451W47IQ8XIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
WATER059QF0KO0RIACT
SODIUM GLUCONATER6Q3791S76IACT
PARSLEY58FMD0Q0EVIACT
GLYCERINPDC6A3C0OXIACT
SODIUM PALM KERNELATE6H91L1NXTWIACT
PALM ACIDB6G0Y5Z616IACT
SODIUM PALMATES0A6004K3ZIACT
PALM KERNEL ACID79P21R4317IACT
SALICYLIC ACIDO414PZ4LPZACTIB
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
FD&C GREEN NO. 33P3ONR6O1SIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
252c2ad3-3aea-ebb8-e063-6394a90ab2efb4e4fb06-29fe-f4a1-e053-2995a90ae7842024-10-23WarningsExact identifier
spl set id: b4e4fb06-29fe-f4a1-e053-2995a90ae784

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.