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Clear Up Prep

Generic Name: salicylic acid
Dosage Form: gel

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 Facts

ACTIVE INGREDIENT

Salicylic Acid 2% w/w.

INACTIVE INGREDIENTS

WATER • SORBITOL • ETHOXYDIGLYCOL • GLYCOLIC ACID • METHYL GLUCETH-20 • SODIUM CITRATE • GLYCERIN • LACTIC ACID • SODIUM HYDROXIDE • CELLULOSE GUM • XANTHAN GUM • ETHYLHEXYLGLYCERIN • PROPYLENE GLYCOL • PHENOXYETHANOL • CITRUS MEDICA LIMONUM (LEMON) FRUIT EXTRACT • HEDERA HELIX (IVY) EXTRACT • SAPONARIA OFFICINALIS EXTRACT •
ARCTIUM LAPPA ROOT EXTRACT • SALVIA OFFICINALIS (SAGE) LEAF EXTRACT •

DIRCETIONS

Cover the eyes with cotton pads soaked in Blue Water. With the fingertips, apply evenly to the face and neck Clear Up Prep Lotion, making sure to avoid the lips.

Application: 2-3 minutes | Pause: 7-8 minutes

WARNINGS

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image of tube 5ml label

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Keep out of reach of children.

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Clear Up Prep 
salicylic acid gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62499-395
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 2 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER  
SORBITOL  
DIETHYLENE GLYCOL MONOETHYL ETHER  
GLYCOLIC ACID  
METHYL GLUCETH-20  
SODIUM CITRATE  
GLYCERIN  
LACTIC ACID  
SODIUM HYDROXIDE  
PROPYLENE GLYCOL  
PHENOXYETHANOL  
CARBOXYMETHYLCELLULOSE SODIUM  
XANTHAN GUM  
ETHYLHEXYLGLYCERIN  
LEMON OIL  
SAPONARIA OFFICINALIS ROOT  
ARCTIUM LAPPA ROOT  
SAGE OIL  
Product Characteristics
Color blue (dark bleu) Score     
Shape Size
Flavor Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:62499-395-11 1 TUBE (TUBE) in 1 CARTON
1 NDC:62499-395-10 5 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 07/01/2010
Labeler - Laboratoire Dr. Renaud (202501565)
Revised: 07/2010
 
Laboratoire Dr. Renaud



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