NDC | 62670-8048-0 |
Set ID | 155b1389-95e0-4056-94ed-e6eeefcfa4f2 |
Category | HUMAN OTC DRUG LABEL |
Packager | Bath & Body Works, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- FLAMMABLE
- DO NOT USE
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR IF
- KEEP OUT OF REACH OF CHILDREN.
-
DIRECTIONS
- shake well and apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water-resistant sunscreen if swimming or sweating
- 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats and sunglasses
- children under 6 months of age: ask a doctor
- OTHER INFORMATION
-
INACTIVE INGREDIENTS
Alcohol Denat., Isobutane, Polyester-8, Butane, Acrylates/Octylacrylamide Copolymer, Ethoxydiglycol, Tocopheryl Acetate, Cocos Nucifera (Coconut) Oil, Butylene Glycol, Fragrance (Parfum), Dimethicone, Trisiloxane, Polyester-10, Propylene Glycol Dibenzoate, Gardenia Tahitensis Flower, Tocopherol, Benzyl Alcohol, Butylphenyl Methylpropional, Citronellol, Coumarin, Limonene, Hydroxycitronellal, Hydroxyisohexyl 3-Cyclohexene Carboxaldehyde.
- COMPANY INFORMATION
- PRODUCT PACKAGING
-
INGREDIENTS AND APPEARANCE
VICTORIAS SECRET SUN BROAD SPECTRUM SPF 25
avobenzone, homosalate, octinoxate, octisalate, octocrylene, oxybenzone aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-8048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3.0 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 13.5 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.6 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 2.4 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 6.0 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62670-8048-0 113 g in 1 CAN Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2015 Labeler - Bath & Body Works, Inc. (878952845) Establishment Name Address ID/FEI Business Operations 220 Labs Inc. 783247950 manufacture(62670-8048)