Label: ACNE CLEANSING PADS- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 58876-102-27 - Packager: DR LIN SKINCARE
- Category: HUMAN OTC DRUG LABEL
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 June 17, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- DO NOT USE
- ASK DOCTOR/PHARMACIST
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
DIRECTIONS
- GENTLY WIPE THE ENTIRE AFFECTED AREA WITH A PAD ONE TO THREE TIMES DAILY.
- DO NOT RINSE.
- BECAUSE EXCESSIVE DRYING OF THE SKIN CAN OCCUR, START WITH ONE APPLICATION DAILY, THENGRADUALLY INCREASE TO TWO TO THREE TIMES DAILY IF NEEDED 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 INGREDIENT
INACTIVE INGREDIENTS
ALOE BARBADENSIS LEAF EXTRACT (ALOE EXTRACT), CAPRYLYL GLYCOL, CITRIC ACID, DISODIUM EDTA, FRAGRANCE, HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT, LAURYL GLUCOSIDE, MENTHOL, PHENOXYETHANOL, PPG-5-CETETH-20, SIMETHICNE, SODIUM BORATE, SODIUM CITRATE, SODIUM LAURYL GLUCOSE CARBOXYLATE, WATER
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE CLEANSING PADS
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58876-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.02 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) WITCH HAZEL (UNII: 101I4J0U34) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) MENTHOL (UNII: L7T10EIP3A) PHENOXYETHANOL (UNII: HIE492ZZ3T) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58876-102-27 70 in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/13/2013 Labeler - DR LIN SKINCARE (622329980) Establishment Name Address ID/FEI Business Operations DIAMOND WIPES INTERNATIONAL, INC. 161104729 manufacture(58876-102) , pack(58876-102)