ACNE SPOT CORRECTOR- benzoyl peroxide cream 
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

BENZYL PEROXIDE 5%

PURPOSE

ACNE TREATMENT

USE

FOR THE TREATMENT OF ACNE AND ACNE DARK AND RED MARKS.

WARNINGS

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

DO NOT USE THIS MEDICATION IF YOU

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.

Other information

• sensitivity test: apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated.

• avoid contact with hair and dyed fabrics, which may be bleached by this product.

STOP USE AND ASK A DOCTOR IF IRRITATION BECOMES SEVERE.

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

DIRECTIONS

INACTIVE INGREDIENTS

Water, Glycerin, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Calendula Extract, Arbutin, Kojic Acid, Ascorbic Acid, Sodium PCA, Allantoin, Panthenol, Sodium Hyaluronate, Glycosphingolipids, Phenoxyethanol, Methylisothiazolinone, Fragrance

QUESTIONS OR COMMENTS?

1-877-445-4624

MON-FRI 8AM - 5PM (PST)

DLSC_AcneSptCorrect_1oz_BOX

DLSC_AcneSptCorrect_1oz_LABEL

ACNE SPOT CORRECTOR 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58876-103
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
CALENDULA OFFICINALIS WHOLE (UNII: PFR03EBU0H)  
ARBUTIN (UNII: C5INA23HXF)  
KOJIC ACID (UNII: 6K23F1TT52)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
ALLANTOIN (UNII: 344S277G0Z)  
PANTHENOL (UNII: WV9CM0O67Z)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
CALENDULOSIDE E (UNII: 184358RYCU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58876-103-3130 mL in 1 TUBE
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(58876-103) , pack(58876-103)

Revised: 6/2013
Document Id: 5f97983e-e7be-472e-a44b-05796179e59a
Set id: e602c70d-a94f-43aa-bb50-f62210600170
Version: 4
Effective Time: 20130625
 
DR LIN SKINCARE