BULL FROG SPF 50 MOSQUITO COAST SUNSCREEN PLUS INSPECT REPELLENT- avobenzone, homosalate, octinoxate, octisalate, octocrylene aerosol, spray

Bull Frog SPF 50 Mosquito Coast Sunscreen Plus Inspect Repellent by

Drug Labeling and Warnings

Bull Frog SPF 50 Mosquito Coast Sunscreen Plus Inspect Repellent by is a Otc medication manufactured, distributed, or labeled by BULLFROG BRANDS, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 3.0%, Octocrylene 5%, Homosalate 10.0%, Octyl Methoxycinnamate 7.5%, Octisalate 5%

Purpose

Sunscreens

Uses

• helps prevent sunburn

Warnings

Skin Alert Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun

For external use only

Do not use

 on damaged or broken skin.

When using this product

 keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

 rash occurs.

Keep out of reach of children.

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

FLAMMABLE:

do not use near heat, flame or while smoking

avoid long term storage above 104°F (40°C)

do not puncture or incinerate

contents under pressure

do not store at temperatures above 120°F (49°C).

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 of age: Ask a doctor

Other information

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

Acrylates/Octylacrylamide Copolymer, SD Alcohol 40 (47% w/w), Aloe Barbadensis Leaf Oil, C12-15 Alkyl Benzoate, Fragrance, Tocopheryl (Vitamin E) Acetate.

Label

INGREDIENTS AND APPEARANCE

BULL FROG SPF 50 MOSQUITO COAST SUNSCREEN PLUS INSPECT REPELLENT 
avobenzone, homosalate, octinoxate, octisalate, octocrylene aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77714-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	50 mg  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
MINERAL OIL (UNII: T5L8T28FGP)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)
SOYBEAN OIL (UNII: 241ATL177A)
ALCOHOL (UNII: 3K9958V90M)
ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77714-007-25	156 g in 1 CAN; Type 0: Not a Combination Product	04/26/2022
2	NDC: 77714-007-22	138 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/02/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	04/26/2022

Labeler - BULLFROG BRANDS, LLC. (117426500)