Equate 2% Salicylic acid Acne treatment pad

Manufacturer
Walmart, Inc.
Effective date
2026-01-19
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:34:03

Label at a glance#

ProductEquate 2% Salicylic acid Acne treatment pad
Active ingredientSALICYLIC ACID
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%

LabelLabel

WARNINGS SECTION

For external use only

OTC - PURPOSE SECTION

Acne medication

OTC - WHEN USING SECTION

  • avoid contact with the eyes. If product gets into the eyes rinse thoroughly with water.
  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • limit use to the face and neck

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center (1-800-222-1222) right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin or eye irritation develops.

OTHER SAFETY INFORMATION

  • do not flush in toilet
  • keep jar lid tightly closed
  • store in cool dry place
  • do not freeze

INDICATIONS & USAGE SECTION

Use for the treatment of acne

OTC - QUESTIONS SECTION

Question? 1-888-287-1915

You may also report side effecs to this phone number.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Clean the skin thorougly before applying this product
  • wipe a pad over the face and neck to cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skinmay occur, start with oneapplication daily, then gradually increase to two or three times daily if needed or as directd by a doctor.
  • if bothersome dryness or peelingoccur, reduce application to once a day or every other day

INACTIVE INGREDIENT SECTION

water, alcohol denat, dipropylene glycol, glycerin, PEG-40 dydrogenated castor oil, sorbitol,fragrance,lavandula angustifolia oil, sodium hydroxide, rose flower oil, disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product ImageProduct Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797892salicylic acid 2 % Medicated PadPSN5
797892salicylic acid 20 MG/ML Medicated PadSCD5
797892salicylic acid 2 % Medicated PadSY5
797892salicylic acid 2 % Topical SwabSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79903-062-012024-03-15C16284748780-11030e365-5ee3-111a-e063-dadaa90a10e2Equate -2% Salicylic Acid Quick Action Pad
79903-062-012024-01-30C16284748780-11030e365-5ee3-111a-e063-dadaa90a10e2Equate -2% Salicylic Acid Quick Action Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-062-01Equate 2% Salicylic acid Acne treatment pad165 g in 1 JARSWAB1655

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-06279903-062-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
Equate 2% Salicylic acid Acne treatment pad2% SALICYLIC ACIDWalmart, Inc.c83c9a42-796a-f322-e053-2995a90a4be92026-01-19WarningsExact identifier
ndc (package): 79903-062-01
ndc (product): 79903-062
ndc11 (package): 79903006201
spl id: 48c4ba7e-9366-6395-e063-6394a90a3080
spl set id: c83c9a42-796a-f322-e053-2995a90a4be9

Reported adverse events (FAERS/openFDA)#

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