DDF  GLYCOLIC EXFOLIATING- salicylic acid gel 
Procter & Gamble Manufacturing Company

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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DDF® Glycolic 10% Exfoliating Oil Control
Exfoliating Oil Control

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Medicine

Uses

  • for the treatment of acne
  • helps clear up acne blemishes
  • helps keep skin clear of new acne blemishes

Warnings

For external use only

Do not use on irritated or broken skin.

When using this product

  • do not use around the eye area. If eye contact occurs, rinse eyes thoroughly with water.
  • 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 physician.
  • avoid unnecessary sun exposure and use a sunscreen.

Stop use and ask a physician if

  • rash, irritation or sensitivity develops or increases.

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

  • cleanse skin thoroughly before applying medication
  • cover entire affected area with a thin layer 1 to 3 times daily
  • because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed, or as directed by a physician
  • if bothersome dryness or peeling occurs, reduce applications to once a day or every other day

Other Information

Sunburn Alert

This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen and limit sun exposure while using this product and for a week afterwards.

Inactive ingredients

water, glycolic acid, alcohol, sodium hydroxide, propylene glycol, polysorbate 80, hydroxyethylcellulose, PEG-40 hydrogenated castor oil, tocopherol, aloe barbadensis leaf juice, disodium EDTA, chamomilla recutita (matricaria) flower extract, vitis vinifera (grape) seed extract, propylene glycol, glycyrrhiza glabra (licorice) root extract, retinyl palmitate, ulmus fulva bark, triethanolamine, zinc gluconate, magnesium aspartate, copper gluconate, sodium ascorbyl phosphate, phenoxyethanol.

Questions or comments?

1-800-818-9770 9:00 AM to 5 PM EST Monday thru Friday

Dist. by HDS Cosmetics Lab, Inc.
New York, NY 10022

PRINCIPAL DISPLAY PANEL - 48 g Bottle Carton

DDF®
DOCTOR'S DERMATOLOGIC FORMULA

GLYCOLIC 10%
EXFOLIATING OIL
CONTROL GEL

SALICYLIC ACID 2%
ACNE TREATMENT

TREAT

  • Controls oily shine
  • Clears and helps prevent
    acne blemishes
  • Visibly reduces
    appearance of pores

ACNE

NET WT. 1.7 OZ. e 48 g

Principal Display Panel - 48 g Bottle Carton
DDF   GLYCOLIC EXFOLIATING
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-700
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)  
glycolic acid (UNII: 0WT12SX38S)  
alcohol (UNII: 3K9958V90M)  
sodium hydroxide (UNII: 55X04QC32I)  
propylene glycol (UNII: 6DC9Q167V3)  
polysorbate 80 (UNII: 6OZP39ZG8H)  
Polyoxyl 40 Hydrogenated Castor Oil (UNII: 7YC686GQ8F)  
tocopherol (UNII: R0ZB2556P8)  
aloe vera leaf (UNII: ZY81Z83H0X)  
Edetate Disodium (UNII: 7FLD91C86K)  
chamomile (UNII: FGL3685T2X)  
vitis vinifera seed (UNII: C34U15ICXA)  
glycyrrhiza glabra (UNII: 2788Z9758H)  
vitamin a palmitate (UNII: 1D1K0N0VVC)  
ulmus rubra bark (UNII: 91QY4PXU8Q)  
trolamine (UNII: 9O3K93S3TK)  
zinc gluconate (UNII: U6WSN5SQ1Z)  
magnesium aspartate (UNII: R17X820ROL)  
copper gluconate (UNII: RV823G6G67)  
sodium ascorbyl phosphate (UNII: 836SJG51DR)  
phenoxyethanol (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-700-481 in 1 CARTON
148 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D01/01/201210/01/2016
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIBusiness Operations
Universal Packaging Systems790530976MANUFACTURE(37000-700)

Revised: 10/2014
 
Procter & Gamble Manufacturing Company