Label: OXY DEEP PORE CLEANSING PADS- salicylic acid swab
-
NDC Code(s):
10742-4204-1,
10742-4204-2,
10742-4204-3,
10742-4204-4, view more10742-4204-5
- Packager: The Mentholatum Company
- 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 April 14, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
When using this product
- keep away from eyes, lips and mouth. If contact occurs, flush 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.
- do not leave pad on skin
-
Directions
- use wipe to clean skin thoroughly
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to 2 or 3 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
Other information
- KEEP TIGHTLY CLOSED
- protect from freezing
- do not flush
- keep away from flame, fire and heat
- avoid storing at temperatures above 100˚F (38˚C)
- Inactive ingredients
- Questions?
- Package/Label Principal Display Panel
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
OXY DEEP PORE CLEANSING PADS
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-4204 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PEG-8/SMDI COPOLYMER (UNII: CCX72L6NY6) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) ISOCETETH-20 (UNII: O020065R7Z) SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2) PENTYLENE GLYCOL (UNII: 50C1307PZG) TROLAMINE (UNII: 9O3K93S3TK) EDETATE TRISODIUM (UNII: 420IP921MB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-4204-1 90 in 1 JAR; Type 0: Not a Combination Product 06/01/2018 2 NDC:10742-4204-2 104 in 1 JAR; Type 0: Not a Combination Product 06/15/2022 3 NDC:10742-4204-3 115 in 1 JAR; Type 0: Not a Combination Product 06/01/2018 4 NDC:10742-4204-4 55 in 1 JAR; Type 0: Not a Combination Product 06/15/2022 5 NDC:10742-4204-5 70 in 1 JAR; Type 0: Not a Combination Product 06/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/01/2018 Labeler - The Mentholatum Company (002105757)