Dermalogica Oil Control

Dosage form: lotion
Ingredients: SALICYLIC ACID 10uL in 1mL
Labeler: PureTek Corporation
NDC Code: 59088-737

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 (1.0%)

Purpose

Acne Treatment

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


Use

Treats acne

Warnings For external use only.

Directions
  • Apply to cleansed face and throat twice daily.
  • Avoid eye area.


Inactive ingredients

Water (Aqua), Butylene Glycol, C12-15 Alkyl Benzoate, Isododecane, Potato Starch Modified, Silica, Hyssopus Officinalis Extract, Melissa Officinalis Leaf Extract, Echinacea Purpurea Extract, Enantia Chlorantha Bark Extract, Yeast Extract, Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Salix Nigra (Willow) Bark Extract, Allantoin, Panthenol, Sodium PCA, Bisabolol, Niacinamide, Ammonium Glycyrrhizate, Zinc Gluconate, Caffeine, Biotin, Phospholipids, Magnesium Ascorbyl Phosphate, Camphor, Menthol, Hamamelis Virginiana (Witch Hazel) Water, Oleanolic Acid, Sodium Hydroxide, Potassium Cetyl Phosphate, Glyceryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Xanthan Gum, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Nylon-12, Glycerin, Disodium EDTA, Ethylhexylglycerin, Phenoxyethanol.

Do not use
  • Do not use around eye area
  • If contact occurs, flush thoroughly with water.
  • if irritation develops, discontinue use

When using this product If dryness or irritation occurs when using other topical acne products at the same time, limit usage to one acne product.

DERMALOGICA OIL CONTROL 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59088-737
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID10 uL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
BUTYLENE GLYCOL 
ALKYL (C12-15) BENZOATE 
ISODODECANE 
STARCH, POTATO 
SILICON DIOXIDE 
MELISSA OFFICINALIS 
ECHINACEA PURPUREA 
YEAST 
HORSE CHESTNUT 
SALIX NIGRA BARK 
ALLANTOIN 
PANTHENOL 
SODIUM PYRROLIDONE CARBOXYLATE 
LEVOMENOL 
NIACINAMIDE 
GLYCYRRHIZIN, AMMONIATED 
ZINC GLUCONATE 
CAFFEINE 
BIOTIN 
LECITHIN, SOYBEAN 
MAGNESIUM ASCORBYL PHOSPHATE 
CAMPHOR (SYNTHETIC) 
MENTHOL 
OLEANOLIC ACID 
SODIUM HYDROXIDE 
POTASSIUM CETYL PHOSPHATE 
GLYCERYL MONOSTEARATE 
POLYOXYL 100 STEARATE 
CETYL ALCOHOL 
XANTHAN GUM 
GLYCERIN 
EDETATE DISODIUM 
ETHYLHEXYLGLYCERIN 
PHENOXYETHANOL 
HAMAMELIS VIRGINIANA LEAF WATER 
HYSSOP 
ANNICKIA CHLORANTHA BARK 
Packaging
#Item CodePackage Description
1NDC:59088-737-051 TUBE (TUBE) in 1 CARTON
160 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/17/2003
Labeler - PureTek Corporation (785961046)
Establishment
NameAddressID/FEIOperations
PureTek Corporation785961046manufacture, label, pack, outsourcing human drug compounding, relabel, repack
Establishment
NameAddressID/FEIOperations
PureTek Corporation031678746manufacture, label, pack, outsourcing human drug compounding, relabel, repack

Revised: 05/2011
 
PureTek Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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