DDF  PROTECT AND CORRECT UV MOISTURIZER SPF 15 - avobenzone, homosalate, octisalate and octocrylene cream 
Procter & Gamble Manufacturing Company

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DDF®
DOCTOR'S DERMATOLOGIC FORMULA

Drug Facts

Active ingredients	Purpose
Avobenzone 3%	Sunscreen
Homosalate 3%	Sunscreen
Octisalate 5 %	Sunscreen
Octocrylene 2.6%	Sunscreen

Use

helps prevent sunburn.

Warnings

For external use only

Do not use on irritated or broken skin.

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

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

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

Directions

• apply evenly before sun exposure and as needed.
• children under 6 months of age: consult a doctor.

Other information

Sun Alert

Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

Inactive ingredients

water, glycerin, niacinamide, polyethylene, acetyl glucosamine, polymethylsilsesquioxane, dimethicone, dimethiconol, sodium acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, polysorbate 80, pentylene glycol, panthenol, mica, titanium dioxide, benzyl alcohol, stearyl alcohol, behenyl alcohol, allantoin, cetyl alcohol, methylparaben, tocopherol, ethylparaben, PEG-100 stearate, cetearyl alcohol, butylene glycol, euterpe oleracea fruit extract, tocopheryl acetate, caprylic/capric triglyceride, macadamia ternifolia seed oil, retinyl palmitate, zea mays (corn) oil, beta-carotene, helianthus annuus (sunflower) seed oil, ubiquinone, palmitic acid, thioctic acid, disodium EDTA, propylparaben, undecylenoyl phenylalanine, iodopropynyl butylcarbamate, stearic acid, mannitol, glutamine, aminopropyl ascorbyl phosphate, propyl gallate, ascorbic acid, camellia sinensis leaf extract, pyridoxine hcl, cyanocobalamin, spirulina platensis extract, glycyrrhiza glabra (licorice) root extract.

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

800.818.9770
www.DDFskincare.com

PRINCIPAL DISPLAY PANEL - 48 g Carton Label

DDF®
DOCTOR'S DERMATOLOGIC FORMULA

PROTECT
AND
CORRECT ™
UV MOISTURIZER
SPF 15

PROTECT

• Helps correct the
  look of discoloration
• Helps prevent future
  hyperpigmentation
  with broad spectrum
  UVA•UVB protection
• Helps even skin tone
  for visible radiance

HYPERPIGMENTATION

NET WT. 1.7 OZ. e 48 g

DDF   PROTECT AND CORRECT UV MOISTURIZER SPF 15 avobenzone, homosalate, octisalate, and octocrylene   cream

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 37000-728 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (Avobenzone) Avobenzone 0.03 g  in 1 g Homosalate (Homosalate) Homosalate 0.03 g  in 1 g Octisalate (Octisalate) Octisalate 0.05 g  in 1 g Octocrylene (Octocrylene) Octocrylene 0.026 g  in 1 g

Inactive Ingredients Ingredient Name Strength water   glycerin   niacinamide   dimethicone   isohexadecane   polysorbate 80   pentylene glycol   panthenol   mica   titanium dioxide   benzyl alcohol   stearyl alcohol   docosanol   allantoin   cetyl alcohol   methylparaben   ethylparaben   polyoxyl 100 stearate   cetostearyl alcohol   butylene glycol   acai   medium-chain triglycerides   macadamia oil   vitamin a palmitate   corn oil   beta carotene   sunflower oil   ubidecarenone   palmitic acid   alpha lipoic acid   edetate disodium   propylparaben   iodopropynyl butylcarbamate   stearic acid   mannitol   glutamine   propyl gallate   ascorbic acid   green tea leaf   pyridoxine hydrochloride   licorice

Product Characteristics Color WHITE Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 37000-728-17 1 BOTTLE In 1 CARTON contains a BOTTLE, PUMP 1 48 g In 1 BOTTLE, PUMP This package is contained within the CARTON (37000-728-17) 2 37000-728-05 1 TUBE In 1 CARTON contains a TUBE 2 14 g In 1 TUBE This package is contained within the CARTON (37000-728-05)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	12/15/2008

Labeler - Procter & Gamble Manufacturing Company (004238200)

Revised: 01/2011Procter & Gamble Manufacturing Company