Label: EQUATE 2% SALICYLIC ACID ACNE TREATMENT PAD- 2% salicylic acid swab
- NDC Code(s): 79903-062-01
- Packager: Walmart, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 15, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WARNINGS
- PURPOSE
-
WHEN USING
- 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
- KEEP OUT OF REACH OF CHILDREN
- STOP USE
- OTHER SAFETY INFORMATION
- INDICATIONS & USAGE
- QUESTIONS
-
DOSAGE & ADMINISTRATION
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
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EQUATE 2% SALICYLIC ACID ACNE TREATMENT PAD
2% salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-062 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 WATER (UNII: 059QF0KO0R) 59.58 g in 100 g Product Characteristics Color Score Shape ROUND (90 patches of 6 cm diameter) Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-062-01 165 g in 1 JAR; Type 0: Not a Combination Product 08/03/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/28/2021 Labeler - Walmart, Inc. (051957769)
