DDF ACNE CONTROL TREATMENT- salicylic acid lotion 
Procter & Gamble Manufacturing Co.

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

Drug Facts

Active ingredient

Salicylic Acid 1.5%

Purpose

Acne Medication

Uses

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

Warnings

For external use only.

When using this product

  • do not get into eyes. If 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.

Do not use on irritated or broken skin.

Stop use and ask a physician if rash, irritation or sensittivity develops and lasts.

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

Directions

  • Cleanse the skin thoroughly before applying medication
  • Cover the 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 doctor
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

water, glycerin, PPG-15 stearyl ether, dimethicone, polymethylsilsesquioxane, decylene glycol, hamamelis virginiana (witch hazel) extract, aloe barbadensis leaf juice, calendula officinalis flower extract, zingiber officinale (ginger) root extract, propylene glycol, tocopheryl acetate, lactic acid, titanium dioxide, polyacrylamide, stearyl alcohol, behenyl alcohol, C13-14 isoparaffin, cetyl alcohol, cetearyl alcohol, cetearyl glucoside, dimethiconol, isohexadecane, steareth-21, laureth-7, disodium EDTA, polyhydroxystearic acid, triethoxycaprylylsilane, PEG-40 hydrogenated castor oil, trideceth-9, sodium benzoate, potassium sorbate.

Dist. by HDS Labs, Inc.
New York, NY 10022

800.818.9770
www.DDFskincare.com

PRINCIPAL DISPLAY PANEL 48 gram Tube Carton

DDF®
DOCTOR'S DERMATOLOGIC FORMULA

ACNE CONTROL
TREATMENT
SALICYLIC ACID
ACNE MEDICATION

  • Fights and controls acne
  • Helps keep pores clear
  • Soothes and restores clarity

ACNE

NET WT. 1.7 OZ. e 48 g

PRINCIPAL DISPLAY PANEL 48 gram Tube Carton
DDF  ACNE CONTROL TREATMENT
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-721
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid0.015 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
glycerin (UNII: PDC6A3C0OX)  
PPG-15 stearyl ether (UNII: 1II18XLS1L)  
dimethicone (UNII: 92RU3N3Y1O)  
decylene glycol (UNII: S57M60MI88)  
hamamelis virginiana top (UNII: UDA30A2JJY)  
aloe vera leaf (UNII: ZY81Z83H0X)  
calendula officinalis flower (UNII: P0M7O4Y7YD)  
ginger (UNII: C5529G5JPQ)  
propylene glycol (UNII: 6DC9Q167V3)  
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
lactic acid (UNII: 33X04XA5AT)  
titanium dioxide (UNII: 15FIX9V2JP)  
stearyl alcohol (UNII: 2KR89I4H1Y)  
docosanol (UNII: 9G1OE216XY)  
C13-14 isoparaffin (UNII: E4F12ROE70)  
cetyl alcohol (UNII: 936JST6JCN)  
cetostearyl alcohol (UNII: 2DMT128M1S)  
isohexadecane (UNII: 918X1OUF1E)  
steareth-21 (UNII: 53J3F32P58)  
laureth-7 (UNII: Z95S6G8201)  
edetate disodium (UNII: 7FLD91C86K)  
triethoxycaprylylsilane (UNII: LDC331P08E)  
polyoxyl 40 hydrogenated castor oil (UNII: 7YC686GQ8F)  
trideceth-9 (UNII: X9HD79I514)  
sodium benzoate (UNII: OJ245FE5EU)  
potassium sorbate (UNII: 1VPU26JZZ4)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-721-171 in 1 CARTON
148 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D06/01/200910/01/2016
Labeler - Procter & Gamble Manufacturing Co. (004238200)

Revised: 10/2014
Document Id: b3eee9a3-4ec5-4340-9927-f45fcdca3541
Set id: f294ee9e-d833-4e39-b25f-2489b9e412fe
Version: 2
Effective Time: 20141009
 
Procter & Gamble Manufacturing Co.