DAILY CLEANSER SALICYLIC ACID ACNE TREATMENT- salicylic acid gel 
DR LIN SKINCARE

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.

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ACTIVE INGREDIENT

SALICYLIC ACID 2%

PURPOSE

ACNE TREATMENT

USE

FOR THE TREATMENT OF ACNE

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE IF YOU HAVE A KNOWN SENSITIVITY TO SALICYLIC ACID OR ASPERIN.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE USING OTHER TOPICAL ACNE MEDICATIONS AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

STOP USE AND ASK A DOCTOR IF SKIN IRRITATION OCCURS.

KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

INACTIVE INGREDIENTS

Water, Sodium Laureth Sulfate, Sodium Cocoamphoacetate, Glycerin, Lauryl Glucoside, Sodium Cocoyl Glutamate, Sodium Lauryl Glucose Carboxylate, Arbutin, Kojic Acid, Ascorbic Acid, Sodium PCA, Allantoin, Panthenol, PEG-150 Distearate, Phenoxyethanol, Aminomethyl Propanol, Methylisothiazolinone, Fragrance

QUESTIONS OR COMMENTS? 1-877-445-4624  MON-FRI  8AM - 5PM (PST)

DLSC_AcneCleanser_8oz_label

DLSC_AcneCleanser_4oz_label

DAILY CLEANSER  SALICYLIC ACID ACNE TREATMENT
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58876-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)  
SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)  
ARBUTIN (UNII: C5INA23HXF)  
KOJIC ACID (UNII: 6K23F1TT52)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
ALLANTOIN (UNII: 344S277G0Z)  
PANTHENOL (UNII: WV9CM0O67Z)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58876-101-18240 mL in 1 BOTTLE
2NDC:58876-101-14120 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D06/13/2013
Labeler - DR LIN SKINCARE (622329980)
Establishment
NameAddressID/FEIBusiness Operations
Westwood Laboratories Inc.069926483manufacture(58876-101) , pack(58876-101)

Revised: 6/2013
Document Id: 25a6216f-6a84-49d8-bd6b-bb2601bd99b0
Set id: 99b45eef-216f-40fc-9b86-68597a6804fd
Version: 2
Effective Time: 20130617
 
DR LIN SKINCARE