Label: VISAGE PRO PEACH FUZZ- sunscreen visage pro peach fuzz 5 emulsion
- NDC Code(s): 35192-047-02
- Packager: CA-Botana International
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 18, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active Ingredient
Avobenzone 2.5%............................................. Sunscreen
Homosalate 7%............................................Sunscreen
Octisalate 5%..............................................Sunscreen
Octocrylene 7%...............................................Sunscreen
Octinoxate 2.5%.............................................Sunscreen
- Purpose
- Ask Doctor
- 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
-
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
- Indications & Usage
- Label
-
INGREDIENTS AND APPEARANCE
VISAGE PRO PEACH FUZZ
sunscreen visage pro peach fuzz 5 emulsionProduct 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)
