COPPERTONE SUNSCREEN OIL FREE SFP 50- avobenzone, homosalate, octisalate, oxybenzone spray

coppertone by

Drug Labeling and Warnings

coppertone by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Each 1mL contains:

Avobenzone 26 mg

Homosalate 118.2 mg

Octisalate 39.43mg

Oxybenzone 52mg

PURPOSE

INDICATIONS & USAGE

DO NOT USE

ASK DOCTOR

ASK DOCTOR/PHARMACIST

WHEN USING

STOP USE

PREGNANCY OR BREAST FEEDING

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

OTHER SAFETY INFORMATION

INACTIVE INGREDIENT

QUESTIONS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

COPPERTONE   SUNSCREEN OIL FREE SFP 50
avobenzone, homosalate, octisalate, oxybenzone spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-7380
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	118.2 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	39.43 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	52 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	26 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-7380-1	177 mL in 1 CAN; Type 0: Not a Combination Product	06/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Export only		06/01/2015

Labeler - Bayer HealthCare LLC. (112117283)