Complexion Protection Moisturizer SPF

.05 oz

1.7 oz

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

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70809-1902-1	50 mL in 1 TUBE; Type 0: Not a Combination Product	07/08/2019
2	NDC:70809-1902-2	12 mL in 1 TUBE; Type 0: Not a Combination Product	02/01/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	07/08/2019

Labeler - USRX LLC (115270633)

Registrant - USRX LLC (115270633)