SUNSCREEN- zinc oxide spray

Sunscreen by

Drug Labeling and Warnings

Sunscreen by is a Otc medication manufactured, distributed, or labeled by Imperfect Foods. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 14%

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

For external use only

Do not use

On damaged or broken skin

Ask Doctor

Stop use and ask a doctor if rash develops

When using

• When using this product keep out of eyes. Rinse with water to remove.
• Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120 degrees F.

Keep out of reach of children

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
• reapply: after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• Spray on hands and apply to face
• use in well-ventilated area
• do not inhale
• children under 6 months: ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum value of 15 or higher along with other sun protection measures including:

• limit time in the sun, especially from 10a.m. - 2 p.m.
• wear long sleeved shirts, pants, hats and sunglasses

Other Information

• Protect this product from excessive heat and direct sun
• may stain some fabrics

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Bentonite, Bisabolol, Butyloctyl Salicylate, Caprylhydroxamic Acid , Caprylic/Capric Triglyceride, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cellulose Gum, Cetearyl Alcohol, Coco-Glucoside, Glycerin, Helianthus Annuus (Sunflower) Oil, Jojoba Esters, Methyl Dihydroabietate, Microcrystalline Cellulose, Polyhydroxystearic Acid, Tocopherol, Water.

Questions or Comments?

1-833-909-2662 Monday - Friday 9am-5pm MST

PRINCIPAL DISPLAY PANEL

SPF 30 Sunscreen Spray NDC: 81757-002-06

INGREDIENTS AND APPEARANCE

SUNSCREEN 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81757-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	14 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENTONITE (UNII: A3N5ZCN45C)
LEVOMENOL (UNII: 24WE03BX2T)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SAFFLOWER OIL (UNII: 65UEH262IS)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81757-002-06	171 g in 1 CAN; Type 0: Not a Combination Product	04/13/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/13/2021

Labeler - Imperfect Foods (109460818)