GRAPEFRUIT SPF 30 BROAD SPECTRUM- sunscreen aerosol

Grapefruit by

Drug Labeling and Warnings

Grapefruit by is a Otc medication manufactured, distributed, or labeled by Bell International Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 1.9%, Octinoxate 7.1%, Octisalate 3.9%, Octocrylene 6.6%

Purpose

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.

Warnings

Flammable Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120 oF.

For external use only

Do not use on damaged or broken skin.

Stop use and ask a doctor if rash occurs.

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

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

Directions

Apply liberally 15 minutes before sun exposure. Spray on skin and rub complete and even coverage. Do not spray on face; spray on hands and rub onto face.

Reapply:

• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours

Sun Protection Measure. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, reguarly use a sunscreen wtih a broad spectrum SPF value of 15 or higher and other sun protection measures including:

• limit time in the sun, especially from 10am-2pm
• wear long-sleeved shirts, pants, hats and sun glasses.

Inactive Ingredients

Actinidia Chinensis (Kiwi) Fruit Extract, Alcohol Denat., Aloe Barbadensis Leaf Huice, Fragrance, Glycerin, Methyl Dihydroabietate, Passiflora Incarnata Extract, Pongamia Glabra Seed Oil, Rubus Idaeus (Raspberry) Fruit Extract

Other Information

protect this product from excessive heat and direct sun.

PDP

INGREDIENTS AND APPEARANCE

GRAPEFRUIT  SPF 30 BROAD SPECTRUM
sunscreen aerosol

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	6.6 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.9 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.1 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3.9 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
RASPBERRY (UNII: 4N14V5R27W)
KARUM SEED OIL (UNII: 62160PU6FJ)
KIWI FRUIT (UNII: 71ES77LGJC)
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)
METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-204-13	178 mL in 1 CAN; Type 0: Not a Combination Product	11/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	11/01/2016

Labeler - Bell International Laboratories, Inc. (967781555)