VISAGE PRO PEACH FUZZ- sunscreen visage pro peach fuzz 5 emulsion

Visage Pro Peach Fuzz by

Drug Labeling and Warnings

Visage Pro Peach Fuzz by is a Otc medication manufactured, distributed, or labeled by CA-Botana International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Avobenzone 2.5%............................................. Sunscreen

Homosalate 7%............................................Sunscreen

Octisalate 5%..............................................Sunscreen

Octocrylene 7%...............................................Sunscreen

Octinoxate 2.5%.............................................Sunscreen

Purpose

Sunscreen

Ask Doctor

Stop use and ask a doctor if rash occurs

Keep out of reach of children

Keep out of reach of children

Inactive Ingredients

.

Acrylates/C10-30 Alkyl Acrylate CrosspolymerC12-15 Alkyl Benzoate, Cetearyl Alcohol, Cetearyl Olivate, Coco-Caprylate/Caprate

Decyl Oleate, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Niacinamide, Phenoxyethanol, Potassium Sorbate,

Sodium Phytate, Sorbitan Olivate, Tocopheryl Acetate, Triethanolamine, Water/Aqua, Xanthan Gum

Safety information

Protect this product from excessive heat and direct sun

Dosage & Administration

Helps prevent sunburn. If used as directed with other sun protection measured decreases the risk of skin cancer and early skin aging caused by the sun. Apply liberally 15 minutes before sun exposure. Usea water resistant sunscreen if swimming or sweating. Reapply : at least 2 hours. Children under 6 months: Ask a doctor. Sun protections measurements. 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 of 15 or higher and othe sun protection measures including: limit time in the sun, specially from 10 a.m.- 2 p.m Wear long-sleeveshirts, pants, hats, and sunglasses. Protect this product from excessive heat and direct 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. If product is swallowed get medical help or contact a poison Control Center right away.

Indications & Usage

Apply liberally 15 minutes before exposure, use water resistant sunscreen, if swimming or sweating. reapply at least every 2 hours. Children under 6 months: ask a doctor

Label

INGREDIENTS AND APPEARANCE

VISAGE PRO PEACH FUZZ 
sunscreen visage pro peach fuzz 5 emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 35192-047
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	7 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.5 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	2.5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
NIACINAMIDE (UNII: 25X51I8RD4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXASODIUM PHYTATE (UNII: ZBX50UG81V)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
XANTHAN GUM (UNII: TTV12P4NEE)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MICA (UNII: V8A1AW0880)
DECYL OLEATE (UNII: ZGR06DO97T)
DIMETHICONE 200 (UNII: RGS4T2AS00)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITAN OLIVATE (UNII: MDL271E3GR)
C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
2,4-D-TROLAMINE (UNII: E6SLK39VZN)
CETYL ALCOHOL (UNII: 936JST6JCN)

Product Characteristics
Color	white (light brownish)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 35192-047-02	113.4 g in 1 PACKAGE; Type 0: Not a Combination Product	07/22/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/22/2022

Labeler - CA-Botana International (106276728)

Establishment
Name	Address	ID/FEI	Business Operations
CA-Botana International		106276728	manufacture(35192-047)