BODY GLOVE SUNSCREEN SPF 30- zinc oxide, titanium dioxide liquid

Body Glove Sunscreen SPF 30 by

Drug Labeling and Warnings

Body Glove Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by SCUBASCREEN LLC, Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Zinc Oxide 6%
Titanium Dioxide 6.2%

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 use near heat, flame, or while smoking. Do not puncture or incinerate. Store at temperature below 120º F (48ºC).
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.

Directions:

• Shake well and apply liberally 15 minutes before sun exposure.
• Hold 4-6 inches away from the skin to apply. Rub in.
• Do not spray directly into face. Spray on hands and apply to face. Avoid breathing mist.
• Use in well-ventilated area.
• 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.
• Sun Protection Measures:Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 am. - 2 pm. 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, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Caprylyl Glycol, Caprylyl/Capryl Glucoside, Carthamus Tinctorious (Safflower) Seed Oil, Decyl Alcohol, Ethylhexylglycerin, Glycerin, Glyceryl Stearate Citrate, Helianthus Annuus (Sunflower) Seed Oil, Hexylene Glycol, Lecithin, Leuconostoc Ferment Filtrate, Oryza Sativa (Rice) Extract, Phenoxyethanol, Polyhydroxystearic Acid, Potassium Sorbate, Punica Granatum Extract, Soybean Peroxidase, Stearic Acid, Superoxide Dismutase, Theobroma Cacao (Cocoa) Seed Butter, Tocopherol, Water (Aqua), Xanthan Gum

Questions?

Call (573) 615-1055

Package Labeling:

INGREDIENTS AND APPEARANCE

BODY GLOVE SUNSCREEN SPF 30 
zinc oxide, titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85763-614
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	60 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (CI 77891 - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
SAFFLOWER OIL (UNII: 65UEH262IS)
DECYL ALCOHOL (UNII: 89V4LX791F)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
SUNFLOWER OIL (UNII: 3W1JG795YI)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
RICE GERM (UNII: 7N2B70SFEZ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
STEARIC ACID (UNII: 4ELV7Z65AP)
SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD)
COCOA BUTTER (UNII: 512OYT1CRR)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85763-614-00	148 mL in 1 CAN; Type 0: Not a Combination Product	05/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/15/2025

Labeler - SCUBASCREEN LLC (123921933)

Registrant - Pure Source, LLC (080354456)