FDA.reportPublic FDA data

Equate

Manufacturer
Walmart INC | Apollo Health and Beauty Care
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:38

Label at a glance#

ProductEquate
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

For the treatment of acne.

Dosage and administration

Wet face. dispense product into hands, lather and massage gently onto face and neck, avoiding the delicate eye area. Rinse thoroughly with warm water and pat dry. because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. if bothersome dryness or peeling occurs, reduce application to once a day or every...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne Medication

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of acne.

Warnings

WARNINGS SECTION

For External use only.

When using this product

OTC - WHEN USING SECTION

  • Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.If irritation occurs, use only one topical acne medication at a time.
  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet face.
  • dispense product into hands, lather and massage gently onto face and neck, avoiding the delicate eye area.
  • Rinse thoroughly with warm water and pat dry.
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Hydrated Silica, PPG-15 Stearyl Ether, Stearyl Alcohol, Glycerin, Distearyldimonium Chloride, Microcrystalline Cellulose, Cetyl Alcohol, Steareth-2, Behenyl Alcohol, Fragrance (Parfum), Steareth-21, Silica, Xanthan Gum, Synthetic Wax, Cetyl Betaine, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Disodium EDTA, Sodium Chloride, Microcrystalline Wax, Sodium Lauryl Sulfate, Blue 1 Lake (CI 42090), Blue 1 (CI 42090).

Questions/comments?

OTC - QUESTIONS SECTION

1-888-287-1915

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
317152salicylic acid 2 % Topical CreamPSN5
317152salicylic acid 20 MG/ML Topical CreamSCD5
317152salicylic acid 2 % Topical CreamSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130194346393435GTIN-13: 0194346393435
EAN-13: 0194346393435
GTIN-12: 194346393435
UPC-A: 194346393435
GTIN storage (14 digits): 00194346393435		PDP.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-317-68Equate200 mL in 1 TUBECREAM2005

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-31779903-317-68

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM7FLD91C86KIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
SALICYLIC ACIDO414PZ4LPZACTIB
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
XANTHAN GUMTTV12P4NEEIACT
WATER059QF0KO0RIACT
SYNTHETIC WAX (540 MW)DW2TC44JRYIACT
HYDRATED SILICAY6O7T4G8P9IACT
STEARETH-2V56DFE46J5IACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
CAPRYLYL GLYCOL00YIU5438UIACT
STEARETH-2153J3F32P58IACT
CETYL ALCOHOL936JST6JCNIACT
BEHENYL ALCOHOL9G1OE216XYIACT
SODIUM CHLORIDE451W47IQ8XIACT
CETYL BETAINEE945X08YA9IACT
SODIUM HYDROXIDE55X04QC32IIACT
STEARYL ALCOHOL2KR89I4H1YIACT
BLUE 1 LAKEJ9EQA3S2JMIACT
SILICAETJ7Z6XBU4IACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
1,2-HEXANEDIOLTR046Y3K1GIACT

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
EquateSALICYLIC ACIDWalmart INC2643feb4-7a29-ef9f-e063-6394a90aec8a2026-05-08WarningsExact identifier
ndc (package): 79903-317-68
ndc (product): 79903-317
ndc11 (package): 79903031768
spl id: 51530352-19a9-0c2a-e063-6294a90ab842
spl set id: 2643feb4-7a29-ef9f-e063-6394a90aec8a

Reported adverse events (FAERS/openFDA)#

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