CLEAR UP CONTROL SOLUTION ANTI-BLEMICHES - salicylic acid gel 
Laboratoire Dr. Renaud

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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Drug Facts

ACTIVE INGREDIENT

Salicylic Acid 2% w/w.

INACTIVE INGREDIENTS

WATER/EAU • ETHOXYDIGLYCOL • GLYCOLIC ACID • METHYL GLUCETH 20 • SODIUM CITRATE • GLYCERIN •
PEG-40 HYDROGENATED CASTOR OIL • SODIUM HYDROXIDE • AMYLOPECTIN • DEXTRIN • LACTIC ACID* • XANTHAN GUM •
BUTYLENE GLYCOL • ARGININE* • CELLULOSE GUM • PEG-60 ALMOND GLYCERIDES • CAPRYLYL GLYCOL • ALLANTOIN •
CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL • ALMOND (PRUNUS AMYGDALUS DULCIS) OIL • ROSEMARY (ROSMARINUS
OFFICINALIS) OIL • SAGE (SALVIA OFFICINALIS) OIL SPANISH • LAVANDIN (LAVANDULA LATIFOLIA) OIL •
COLEUS FORSKOHLII OIL • GALANGAL (KAEMPFERIA GALANGA) EXTRACT • CHAMOMILE (ANTHEMIS NOBILIS) OIL •
CARBOMER • NORDIHYDROGUAIARETIC ACID • OLEANOLIC ACID • ETHYLHEXYL GLYCERIN • PHENOXYETHANOL

For the treatment of acne.Reduces the number of acne pimples,blackheads and whiteheads and allows skin to heal.

DIRECTIONS

Morning and evening, first
cleanse the skin thoroughly with CLEAR UP
Cleansing Gel. Then apply a thin layer
of CLEAR UP Control Solution Anti-Blemishes
to the entire face and other affected areas
one to three times daily, or as directed by a
doctor. Massage in with light effleurages.
Then apply CLEAR UP Anti-Shine Moisturizer
SPF 15. 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.

WARNINGS

For external use only. 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.
Avoid direct contact with the eyes. If product
gets into the eyes, rinse liberally with water.
Discontinue use if skin irritation develops
or increases. If irritation persists, consult a
doctor. This product contains alpha-hydroxyacids
(AHA) which may increase sensitivity
to the sun and lead to skin burn. Reduce sun
exposure and use a sunblock during the use
of this product and the week following its use.

image of tube 50ml lable
image of tube 50ml lable

image of tube 15 ml lable
image of tube 15 ml lable

image of carton 50ml label
image of carton 50ml lable


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Keep out of reach of children.
CLEAR UP CONTROL SOLUTION ANTI-BLEMICHES 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62499-392
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
AMYLOPECTIN (UNII: 4XO4QFV777)  
OLEANOLIC ACID (UNII: 6SMK8R7TGJ)  
LACTIC ACID (UNII: 33X04XA5AT)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
XANTHAN GUM (UNII: TTV12P4NEE)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ARGININE (UNII: 94ZLA3W45F)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ALLANTOIN (UNII: 344S277G0Z)  
ORANGE OIL (UNII: AKN3KSD11B)  
ALMOND OIL (UNII: 66YXD4DKO9)  
ROSEMARY OIL (UNII: 8LGU7VM393)  
SAGE OIL (UNII: U27K0H1H2O)  
LAVANDIN OIL (UNII: 9RES347CKG)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)  
Product Characteristics
Colorblue (DRAK BLEU) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62499-392-111 in 1 CARTON
1NDC:62499-392-0450 g in 1 TUBE
2NDC:62499-392-121 in 1 KIT
2NDC:62499-392-0615 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H06/29/2010
Labeler - Laboratoire Dr. Renaud (202501565)
Registrant - Laboratoire Dr. Renaud (202501565)
Establishment
NameAddressID/FEIBusiness Operations
Laboratoire Dr. Renaud202501565manufacture

Revised: 6/2010
Document Id: 0786cbe9-dc97-45e2-b3b0-35a2aa08db31
Set id: 4c35ec41-4e10-415d-840c-3aa802d95021
Version: 1
Effective Time: 20100629
 
Laboratoire Dr. Renaud