BIOSOLIS FACE SUNSCREEN BROAD SPECTRUM SPF30- zinc oxide cream

BIOSOLIS Face Sunscreen broad spectrum SPF30 by

Drug Labeling and Warnings

BIOSOLIS Face Sunscreen broad spectrum SPF30 by is a Otc medication manufactured, distributed, or labeled by Pro Vera SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Zinc oxide 18.8%

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

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 Poison Control Center right away

Directions

• apply liberally 15 minutes before sun exposure
• 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 aBroad Spectrum SPF value of 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m. – 3 p.m.
• wear long-sleeved shirts, pants, hats and sunglasses
• reapply
• after 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

ALOE VERA LEAF JUICE*, BENZYL ALCOHOL,BISABOLOL*, CAPRYLIC/CAPRIC TRIGLYCERIDE,DEHYDROACETIC ACID, DICAPRYLYL CARBONATE,HYDROGENATED VEGETABLE OIL, KARANJATREE SEED EXTRACT, POLYGLYCERYL-2DIPOLYHYDROXYSTEARATE, POLYGLYCERYL-3DIISOSTEARATE, POLYHYDROXYSTEARIC ACID,PROPANEDIOL, SESAME OIL*, SODIUM CHLORIDE,TOCOPHEROL, WATER.

Questions or comments?

1-866-853-9427

Package Labeling:61296-018-00

INGREDIENTS AND APPEARANCE

BIOSOLIS FACE SUNSCREEN BROAD SPECTRUM SPF30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61296-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	188 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LEVOMENOL (UNII: 24WE03BX2T)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
PONGAMIA PINNATA SEED (UNII: C2BRV53B1V)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PROPANEDIOL (UNII: 5965N8W85T)
SESAME OIL (UNII: QX10HYY4QV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61296-018-00	1 in 1 BOX	01/07/2022	12/31/2024
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/07/2022	12/31/2024

Labeler - Pro Vera SA (375713286)

Registrant - Pro Vera SA (375713286)