PEAR SPF 30 BROAD SPECTRUM- sunscreen aerosol

Pear by

Drug Labeling and Warnings

Pear 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

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 temperatues 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 with 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 for complete and even coverage. Do not spray on face; spray on hands and rub onto face.

Reapply:

• After 80 minutes of swimming or sweating
• Immiately after towel drying
• At least every 2 hours

Children under 6 months: Ask a doctor.

Sun Protection Measure. 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 protetion 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 Juice, Fragrance, Glycerin, Methyl Dihydroabietate, Passiflora Incarnata Extract, Pongamia Glabra Seed Oil, Rubus Idaeus (Raspberry) Fruit Extract

Other Inforamtion

Protect this product from excessive heat and direct sun

PDP

INGREDIENTS AND APPEARANCE

PEAR  SPF 30 BROAD SPECTRUM
sunscreen aerosol

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76150-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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
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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76150-205-13	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)