COPPERTONE TANNING DEFEND AND GLOW SPF 8- octinoxate and octocrylene lotion

Coppertone Tanning Defend and Glow SPF 8 by

Drug Labeling and Warnings

Coppertone Tanning Defend and Glow SPF 8 by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active ingredients

Active ingredients

Octinoxate 7%, Octocrylene 3%

Purpose

Purpose

Sunscreen

Uses

Uses

■ helps prevent sunburn

Warnings

Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

For external use only

Do not use

Do not use on damaged or broken skin

When using this product

When using this product keep out of eyes. Rinse with water to remove.

Stop use

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

■ apply liberally 15 minutes before sun exposure

■ reapply:

■ after 80 minutes of swimming or sweating

■ immediately after towel drying

■ at least every 2 hours

■ children under 6 months: Ask a doctor

Other information

Other information

■ protect this product from excessive heat and direct sun

■ may stain or damage some fabrics or surfaces

Inactive ingredients

Inactive ingredients water, sorbitol, ethylhexyl palmitate, benzyl alcohol, cetyl phosphate, acrylates/C10-30 alkyl acrylate crosspolymer, dimethicone, tocopherol (vitamin E), triethanolamine, aloe barbadensis leaf extract, fragrance, carbomer, chlorphenesin, disodium EDTA

Questions

Questions? 1-866-288-3330

Package label

New Look

Coppertone®

Sunscreen Lotion

Tanning

Defend & Glow™

Antioxidant Enriched 8

Water Resistant

(80 Minutes)

SPF 8

INGREDIENTS AND APPEARANCE

COPPERTONE TANNING DEFEND AND GLOW SPF 8 
octinoxate and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-7417
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	70.175 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	30.075 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CETYL PHOSPHATE (UNII: VT07D6X67O)
TOCOPHEROL (UNII: R0ZB2556P8)
CHLORPHENESIN (UNII: I670DAL4SZ)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Product Characteristics
Color	white (White to off white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-7417-1	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2017	09/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/01/2017	09/01/2020

Labeler - Bayer HealthCare LLC. (112117283)