Label: BLEMISH CLEARING FACIAL WIPES- salicylic acid cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 69840-001-01, 69840-001-02 - Packager: Yes To Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 27, 2021
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only
- Avoid contact with the eyes.
Before using for the first time, apply a small amount to the affected area for 3 days. If no discomfort occurs, then follow directions for use. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
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Directions
Wipe the entire effected area one to three times daily. 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.
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Inactive Ingredients
Water (Aqua), Glycerin, Betaine, Solanum Lycopersicum (Tomato) Fruit Extract1, Aspalathus Linearis (Red Tea) Leaf Extract, Polyglyceryl-4 Caprate, Caprylyl/Capryl Glucoside, Hamamelis Virginiana (Witch Hazel) Extract, Citrullus Vulgaris (Watermelon) Fruit Extract, Capiscum Frutescens (Red Pepper) Fruit Extract, Galactoarabinan, Alcohol, Citric Acid, Sodium Hydroxide, Sodium Benzoate, Potassium Sorbate, Phenoxyethanol, Fragrance (Parfum).
- 1
- Certified Organic Ingredient
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- PRINCIPAL DISPLAY PANEL - 40 Wipe Packet
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INGREDIENTS AND APPEARANCE
BLEMISH CLEARING FACIAL WIPES
salicylic acid clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69840-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 10 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BETAINE (UNII: 3SCV180C9W) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) TOMATO (UNII: Z4KHF2C175) WATERMELON (UNII: 231473QB6R) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) CAPSICUM (UNII: 00UK7646FG) ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU) GALACTOARABINAN (UNII: SL4SX1O487) ALCOHOL (UNII: 3K9958V90M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) Product Characteristics Color WHITE Score no score Shape RECTANGLE Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69840-001-01 25 in 1 PACKET; Type 0: Not a Combination Product 05/20/2015 01/01/2018 2 NDC:69840-001-02 40 in 1 PACKET; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 05/20/2015 Labeler - Yes To Inc. (788689680) Establishment Name Address ID/FEI Business Operations Albaad USA Inc. 143406457 MANUFACTURE(69840-001)
