FACET DAILY MOISTURIZER SPF 35- avobenzone, octocrylene, octisalate, octinoxate lotion

Facet Daily Moisturizer SPF 35 by

Drug Labeling and Warnings

Facet Daily Moisturizer SPF 35 by is a Otc medication manufactured, distributed, or labeled by Cosco International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient....................Purpose

Avobenxone 3.00%..................Sunscreen

Octocrylene 9.50%..................Sunscreen

Octilsalate 5.00%....................Sunscreen

Octinoxate 7.50%....................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.
• Higher SPF gives more subburn protection

Warnings

For external use only.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

When using this product 

• keep out of eyes.  Rinse with water to remove.

Do not use

• on damaged or broken skin.

Stop use and ask a doctor if

• rash or irritation develops and lasts.

Directions

• Use only as directed
• Apply liberally and spread evenly 15 minutes before sun exposure
• Reapply at least every 2 hours or immediately after towel drying
• Use a water-resistant sunscreen if swimming or sweating
• For children under 6 months of age:  Ask a doctor

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 the sun, especially from 10 a.m. - 2 p.m.
• Wear long-sleeved shirts, pants, hats and sunglasses.

Inactive Ingredients

Water, Glyceryl Stearate SE, Alkyl (C12-15) Benzoate, Butyloctyl Salicylate, Capryloyl Glycerin/Sebacic Acid Copolymer, Glyceryl Stearate/PEG-100 Stearate, Cetostearyl Alcohol, Ceteareth 20, Isopropyl Myristate, Dimethicone, Phenoxyethanol, Butylene Glycol, Glycerin, Jojoba Oil, Caprylyl Glycol, Carbomer Interpolymer Type B (Allyl Pentaerythritol Crosslinked), Niacinamide (vitamin B3), Panthenol, Sodium Chloride, Sodium Hydroxide, Sodium Hyaluronate, Hyaluronic Acid

Other Information

• Protect the product in this container from excessuve heat and direct sun
• Store at temperatures below 90°F
• May discolor some fabrics.

Questions or Comments?

Call (855) 658-8855

Distributed by

Thirty Madison

New York, NY, 1001

(855) 658-8855

Made in USA

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FACET DAILY MOISTURIZER SPF 35 
avobenzone, octocrylene, octisalate, octinoxate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52261-0800
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.03 kg  in 1 kg
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.05 kg  in 1 kg
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.095 kg  in 1 kg
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.075 kg  in 1 kg

Inactive Ingredients
Ingredient Name	Strength
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
PANTHENOL (UNII: WV9CM0O67Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
HYALURONIC ACID (UNII: S270N0TRQY)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
JOJOBA OIL (UNII: 724GKU717M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52261-0800-1	1 in 1 CARTON	09/01/2022
1		0.059 kg in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 52261-0800-0	0.003 kg in 1 PACKET; Type 0: Not a Combination Product	09/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	09/01/2022

Labeler - Cosco International, Inc. (016433141)

Registrant - Cosco International, Inc. (016433141)

Establishment
Name	Address	ID/FEI	Business Operations
Cosco International, Inc.		016433141	manufacture(52261-0800) , label(52261-0800) , pack(52261-0800)