COMPLEXION PROTECTION MOISTURIZER SPF- benzophenone, avobenzone, octinoxate, octisalate cream cream

Complexion Protection Moisturizer SPF by

Drug Labeling and Warnings

Complexion Protection Moisturizer SPF by is a Otc medication manufactured, distributed, or labeled by USRX LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT -

Benzophenone 3.6%

Avobenzone 1%

Octinoxate 7.5%

Octisalate 5%

Sunscreen

FOR EXTERNAL USE ONLY

DO NOT USE - On damaged or broken skin

STOP USE AND ASK A DOCTOR IF A RASH OCCURRS

Aqua (Water), Caprylic/Capric Triglyceride, Corn Starch Modified, Cetearyl Olivate, Diethylhexyl 2,6-Naphthalate, C12-15 Alkyl Benzoate, Sorbitan Olivate, Gluconolactone, Squalane, Glycerin, Cyclopentasiloxane, Tocopheryl Acetate (D-alpha), Sodium Hyaluronate (L), Xanthan Gum, Carbomer, Aminomethyl Propanol, Sodium Benzoate, Phenethyl Alcohol, Caprylyl Glycol, Phenoxyethanol, Trisodium Ethylenediamine Disuccinate, Potassium Sorbate​

INGREDIENTS AND APPEARANCE

COMPLEXION PROTECTION MOISTURIZER SPF 
benzophenone, avobenzone, octinoxate, octisalate cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70809-1902
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 mg  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1 mg  in 100 mL
BENZOPHENONE (UNII: 701M4TTV9O) (BENZOPHENONE - UNII:701M4TTV9O)	BENZOPHENONE	3.6 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
STARCH, CORN (UNII: O8232NY3SJ)
WATER (UNII: 059QF0KO0R)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
GLYCERIN (UNII: PDC6A3C0OX)
SQUALANE (UNII: GW89575KF9)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SORBITAN OLIVATE (UNII: MDL271E3GR)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70809-1902-1	50 mL in 1 TUBE; Type 0: Not a Combination Product	07/08/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/08/2019

Labeler - USRX LLC (115270633)

Registrant - USRX LLC (115270633)