NDC | 58668-9611-1, 58668-9611-2, 58668-9611-3, 58668-9611-4 |
Set ID | 432f07e8-6f0f-4946-b1b6-4559ef1af561 |
Category | HUMAN OTC DRUG LABEL |
Packager | Laboratoires Clarins |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Drug Facts
- Active ingredients
- Uses:
- Warnings:
-
Directions:
• apply liberally 15 minutes before sun exposure
• apply to all skin exposed to the sun
• children under 6 months: Ask a doctor
• 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 broad spectrum SPF 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
• reapply at least every 2 hours
• use a water resistant sunscreen if swimming or sweating -
Inactive ingredients
AQUA/WATER/EAU, GLYCERIN, BUTYLOCTYL SALICYLAET, DIMETHICONE, C12-15 ALKYL BENZOATE, CETEARYL ALCOHOL, PROPANEDIOL, POTASSIUM CETYL PHOSPHATE, PARFUM/FRAGRANCE, CELLULOSE, CETEARYL GLUCOSIDE, DIPSACUS SYLVESTRIS EXTRACT, PHENOXYETHANOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CAPRYLYL GLYCOL, CI77891/TITANIUM DIOXIDE, TROMETHAMINE, SYNTHETIC FLUORPHLOGOPITE, DISODIUM EDTA, TOCOPHERYL ACETATE, XANTHAN GUM, SODIUM HYALURONATE, DIMETHICONOL, TOCOPHEROL, BUTYLENE GLYCOL, DIOSPYROS MESPILIFORMIS LEAF EXTRACT, MALTODEXTRIN, SANICULA EUROPAEA EXTRACT, MYROTHAMNUS FLABELLIFOLIA EXTRACT, CITRIC ACID, LAPSANA COMMUNIS FLOWER/LEAF/STEM EXTRACT, FURCELLARIA LUMBRICALIS EXTRACT, SODIUM CITRATE, POTASSIUM SORBATE, ASCORBIC ACID, GLYCOLIC ACID, LACTIC ACID, MARIS SAL/SEA SALT/SEL MARIN, CI14700/RED, CI17200/RED33, POLYVINYL ALCOHOL, COPPER PALMITOYL HEPTAPEPTIDE-14, HEPTAPEPTIDE-15 PALMITATE [S2912A]
- Other information:
- Questions or comments?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
MULTI-ACTIVE JOUR SPF 20 BROAD SPECTRUM SUNSCREEN
avobenzone,homosalate,octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58668-9611 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 27 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIMETHICONE (UNII: 92RU3N3Y1O) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) POWDERED CELLULOSE (UNII: SMD1X3XO9M) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TROMETHAMINE (UNII: 023C2WHX2V) EDETATE DISODIUM (UNII: 7FLD91C86K) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XANTHAN GUM (UNII: TTV12P4NEE) HYALURONATE SODIUM (UNII: YSE9PPT4TH) TOCOPHEROL (UNII: R0ZB2556P8) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIOSPYROS MESPILIFORMIS LEAF (UNII: 0R6X2JX6J1) MALTODEXTRIN (UNII: 7CVR7L4A2D) SANICULA EUROPAEA LEAF (UNII: JYZ6110L9I) MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5) LAPSANA COMMUNIS FLOWERING TOP (UNII: T9B77O7PZA) FURCELLARIA LUMBRICALIS (UNII: GRS9V5FVR9) SODIUM CITRATE (UNII: 1Q73Q2JULR) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) ASCORBIC ACID (UNII: PQ6CK8PD0R) GLYCOLIC ACID (UNII: 0WT12SX38S) WATER (UNII: 059QF0KO0R) LACTIC ACID (UNII: 33X04XA5AT) SEA SALT (UNII: 87GE52P74G) FD&C RED NO. 4 (UNII: X3W0AM1JLX) D&C RED NO. 33 (UNII: 9DBA0SBB0L) POLYVINYL ALCOHOL (UNII: 532B59J990) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58668-9611-1 1 in 1 BOX 09/24/2015 12/15/2019 1 50 mL in 1 JAR; Type 0: Not a Combination Product 2 NDC:58668-9611-2 2 mL in 1 PACKET; Type 0: Not a Combination Product 09/24/2015 12/15/2019 3 NDC:58668-9611-3 2 mL in 1 PACKET; Type 0: Not a Combination Product 09/24/2015 12/15/2019 4 NDC:58668-9611-4 1 in 1 CARTON 09/24/2015 12/15/2019 4 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 09/24/2015 Labeler - Laboratoires Clarins (266317555)