DDF MATTIFYING MOISTURIZER  BROAD SPECTRUM SPF 15- avobenzone, homosalate, octisalate, and octocrylene lotion 
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 Mattifying Oil Control Moisturizer
Broad Spectrum SPF 15

Drug Facts

Active ingredientsPurpose
Avobenzone 3.0%Sunscreen
Homosalate 3.0%Sunscreen
Octisalate 5.0%Sunscreen
Octocrylene 2.6%Sunscreen

Uses

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

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

Directions

  • apply liberally 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use water resistant sunscreen if swimming or sweating
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in sun, especially from 10 a.m.- 2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses
  • children under 6 months: ask a doctor

Other information

  • protect this product from excessive heat and direct sun

Inactive ingredients

water, glycerin, polyethylene, dimethicone, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, pentylene glycol, panthenol, stearyl alcohol, behenyl alcohol, cetyl alcohol, tocopheryl acetate, sodium dehydroacetate, hamamelis virginiana (witch hazel) extract, calendula officinalis flower extract, aloe barbadensis leaf juice, zingiber officinale (ginger) root extract, retinyl palmitate, benzyl alcohol, dimethiconol, PEG-100 stearate, cetearyl glucoside, cetearyl alcohol, disodium EDTA, sodium hyaluronate, iodopropynyl butylcarbamate, polysorbate 60, triethanolamine, ethylparaben, methylparaben, propylparaben, isohexadecane, stearic acid, titanium dioxide.

PRINCIPAL DISPLAY PANEL - 48 g Tube Carton

DDF®
DOCTOR'S DERMATOLOGIC FORMULA

MATTIFYING OIL
CONTROL
MOISTURIZER
WITH SUNSCREEN
BROAD SPECTRUM SPF 15

PROTECT

  • Helps balance shine
  • Minimizes imperfections
  • Helps protect from UVA•UVB
    sun damage

ACNE

HOWARD SOBEL, MD
Founder

NET WT. 1.7 OZ. e 48 g

PRINCIPAL DISPLAY PANEL - 48 g Tube Carton
DDF MATTIFYING MOISTURIZER   BROAD SPECTRUM SPF 15
avobenzone, homosalate, octisalate, and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-705
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone0.03 g  in 1 g
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate0.03 g  in 1 g
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate0.05 g  in 1 g
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene0.026 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
glycerin (UNII: PDC6A3C0OX)  
high density polyethylene (UNII: UG00KM4WR7)  
dimethicone (UNII: 92RU3N3Y1O)  
pentylene glycol (UNII: 50C1307PZG)  
panthenol (UNII: WV9CM0O67Z)  
stearyl alcohol (UNII: 2KR89I4H1Y)  
docosanol (UNII: 9G1OE216XY)  
cetyl alcohol (UNII: 936JST6JCN)  
.alpha.-tocopherol acetate (UNII: 9E8X80D2L0)  
sodium dehydroacetate (UNII: 8W46YN971G)  
hamamelis virginiana top (UNII: UDA30A2JJY)  
calendula officinalis flower (UNII: P0M7O4Y7YD)  
aloe vera leaf (UNII: ZY81Z83H0X)  
ginger (UNII: C5529G5JPQ)  
vitamin a palmitate (UNII: 1D1K0N0VVC)  
benzyl alcohol (UNII: LKG8494WBH)  
PEG-100 stearate (UNII: YD01N1999R)  
cetearyl glucoside (UNII: 09FUA47KNA)  
cetostearyl alcohol (UNII: 2DMT128M1S)  
edetate disodium (UNII: 7FLD91C86K)  
hyaluronate sodium (UNII: YSE9PPT4TH)  
iodopropynyl butylcarbamate (UNII: 603P14DHEB)  
polysorbate 60 (UNII: CAL22UVI4M)  
trolamine (UNII: 9O3K93S3TK)  
ethylparaben (UNII: 14255EXE39)  
methylparaben (UNII: A2I8C7HI9T)  
propylparaben (UNII: Z8IX2SC1OH)  
isohexadecane (UNII: 918X1OUF1E)  
stearic acid (UNII: 4ELV7Z65AP)  
titanium dioxide (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-705-481 in 1 CARTON
148 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:37000-705-2828 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35211/01/201210/01/2016
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIBusiness Operations
UPSI (Diversapack of California)177711082MANUFACTURE(37000-705)

Revised: 10/2014
Document Id: 348200c3-e5df-4c3d-83e8-04b31b3c7412
Set id: df036a25-fc38-4f5f-adf0-0633001f7097
Version: 2
Effective Time: 20141009
 
Procter & Gamble Manufacturing Company