NDC | 58443-0131-4 |
Set ID | 85bee94f-2de3-4d7d-8c09-ec23206ed6f7 |
Category | HUMAN OTC DRUG LABEL |
Packager | Prime Enterprises, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredients
- Purpose
- Uses
- Warnings
-
Directions:
- 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 & early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher & other sun protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
-
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Butylphthalimide, C12-15 Alkyl Benzoate , Calendula Officinalis Flower Extract, Caramel, Ceteareth-20, Cetyl Alcogol, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Dihydroxyacetone, Dimethicone, Disodium EDTA, Erythrulose, Fragrance (Parfum), Glycerin, Glyceryl Dilaurate, Isopropylphthalimide, Methylisothiazolinone, Phenoxyethanol, Polyethylene, Polyquaternium-37, PPG-1 Trideceth-6, Propylene Glycol, Propylene Glycol Dicaprylate/Dicaprate, Stearyl Alcohol, Tocopheryl Acetate, Water (Aqua)
- Other information
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 177 mL Tube Label
-
INGREDIENTS AND APPEARANCE
ULTA SPF 15 MEDIUM DEEP BROAD SPECTRUM TINTED SUNSCREEN
avobenzone, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58443-0131 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 19.6 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 49 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 18.13 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E) ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CARAMEL (UNII: T9D99G2B1R) CETEARETH-22 (UNII: 28VZG1E234) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID ACETATE (UNII: DSO12WL7AU) DIHYDROXYACETONE (UNII: O10DDW6JOO) DIMETHICONE (UNII: 92RU3N3Y1O) EDETATE DISODIUM (UNII: 7FLD91C86K) L-ERYTHRULOSE (UNII: WKK1W5B83O) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL DILAURATE (UNII: MFL3ZIE8SK) PHENOXYETHANOL (UNII: HIE492ZZ3T) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) POLYQUATERNIUM-37 (3000 MPA.S) (UNII: HU373G0YSU) PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY) PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) WATER (UNII: 059QF0KO0R) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58443-0131-4 177 mL in 1 TUBE; Type 0: Not a Combination Product 11/25/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 11/25/2013 Labeler - Prime Enterprises, Inc. (101946028) Registrant - Prime Enterprises, Inc. (101946028) Establishment Name Address ID/FEI Business Operations Prime Enterprises, Inc. 101946028 label(58443-0131) , pack(58443-0131) , manufacture(58443-0131) , analysis(58443-0131)