DE-AGING MOISTURIZING DAY CREME WITH SUNSCREEN SPF 20- octinoxate, octisalate, oxybenzone, titanium dioxide cream

De-Aging Moisturizing Day Creme With Sunscreen SPF 20 by

Drug Labeling and Warnings

De-Aging Moisturizing Day Creme With Sunscreen SPF 20 by is a Otc medication manufactured, distributed, or labeled by Market America. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients                               Purpose
Octinoxate 7.5%..............................  Sunscreen
Octisalate 3.0%................................  Sunscreen
Oxybenzone 3.0%............................. Sunscreen
Titanium Dioxide 0.4%.......................Sunscreen

PURPOSE

Uses  Helps prevent sunburn  Higher SPF gives more sunburn protection.

WARNINGS

Warnings For External use only

DO NOT USE

Do not use on irritated or broken skin.

STOP USE

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

WHEN USING

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions  - Apply to clean skin for daily sun protection  - Allow to absorb  - Ask a doctor before use on children under 3 years of age.

OTHER SAFETY INFORMATION

Other Information  Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

INACTIVE INGREDIENT

Inactive Ingredients: Water, Propylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, C12-15 Alkyl Benzoate, Sodium Hyaluronate, Butylene Glycol, Ceramide 2, Human Oligcpeptide-9, Teprenonal, Lonicers Caprifolium (Honeysuckle) Flower Extract, Zizyphus Jujuba Fruit Extract, Glycymhiza Glabra (licorice) Root Extract, Retinyl Palmitate, Tocopheryl Acetate, Cetyl Alcohol Dimethicone, Alumina, Allantein, Panthenol, Sodium PCA, Lecithin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Sodium Phosphate, Sodium Chloride, EDTA, Disodium EDTA, Phenoxyethanol, Caprylyl Glycol, Fragrance.

DESCRIPTION

De-Aging Moisturing Day Creme  With Sunscreen SPF 20  This light and oil-free creme may be used as a base for makeup application. Promotes ultimate hydration for smoother, healthier-looking skin.

PRINCIPAL DISPLAY PANEL

ceLLuLaR laboratories  net vol. 2 fl. oz./60 mL

PRINCIPAL DISPLAY PANEL

Manufactured for and exclusively distributed in the U.S. by: Market America, Inc. 1302 Pleasant Ridge Road Greensboro, NC 27409  Imported and exclusively distributed by: Market Hong Kong, Inc., in Hong Kong  Unit 1615-1620, Level 16, Tower II Grend Century Place 193 Prince Edward Road West Mongkok, Kowloon, Hong Kong.  Market America, Inc., in Canada 100 Wilkinson Road, Unit 5-6 Brampton, Ontario L6T 4Y9.  Market Australia, Inc., in Australia Unit 2/36 Liverpool St. Ingleburn, NSW 2565

PRINCIPAL DISPLAY PANEL

Drug Facts

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Drug Facts (continued)

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INGREDIENTS AND APPEARANCE

DE-AGING MOISTURIZING DAY CREME WITH SUNSCREEN SPF 20 
octinoxate, octisalate, oxybenzone, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76209-234
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	30 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	30 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
STEARIC ACID (UNII: 4ELV7Z65AP)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CERAMIDE 2 (UNII: C04977SRJ5)
JUJUBE FRUIT (UNII: G55HNL2C70)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALUMINUM OXIDE (UNII: LMI26O6933)
PANTHENOL (UNII: WV9CM0O67Z)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM PHOSPHATE (UNII: SE337SVY37)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETIC ACID (UNII: 9G34HU7RV0)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76209-234-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/19/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	06/08/2011

Labeler - Market America (797412236)

Establishment
Name	Address	ID/FEI	Business Operations
Englewood Lab, Inc.		080366903	manufacture(76209-234)

Establishment
Name	Address	ID/FEI	Business Operations
Englewood Lab Korea Co., Ltd.		690104005	manufacture(76209-234)