DIAMOND LUMINOUS UV DEFENSE LIGHT TINTED FLUID SUNSCREEN BROAD SPECTRUM SPF 40- titanium dioxide, zinc oxide lotion 
NATURA BISSE INTERNATIONAL SA

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Diamond Luminous UV Defense Light Tinted Fluid Sunscreen Broad Spectrum SPF 40

Drug Facts

Active ingredients

Titanium dioxide 7.8%

Zinc oxide 25%

Purpose

Sunscreen

Uses

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.

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure.

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 other sun protection measures including: Sun Protection Measures.

Other information

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

Water, C15-19 Alkane, Butyloctyl Salicylate, Niacinamide, Dimethicone, Coco-Caprylate Propanediol, PEG-30 Dipolyhydroxystearate, Caprylic/Capric Triglyceride, Polyglyceryl-6 Polyricinoleate, Polyglyceryl-6 Polyhydroxystearate, Diisopropyl Sebacate, Polyhydroxystearic Acid, Sodium Chloride, Silica, Tocopheryl Acetate, Arginine, Artemia Extract, Tocopherol, Lysine, Ascorbyl Palmitate,Triethoxycaprylylsilane, Stearalkonium Hectorite, Polyglycerin-6, Disodium EDTA, Propylene Carbonate, Cetyl Alcohol, Ethylhexylglycerin, Sodium Lauroyl Glutamate, Magnesium Chloride, Phenoxyethanol, Potassium Sorbate, Fragrance, Iron Oxides.

Questions?

1-800-762-8872 M-F 9:00 AM to 5:00 PM

Package Labeling:63730-001-01

63730-001-01 Label

Package Labeling:63730-001-02

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Package Labeling:63730-001-03

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Package Labeling:63730-001-04

63730-001-04 outer label63730-001-04 inner label63730-001-04 label

DIAMOND LUMINOUS UV DEFENSE LIGHT TINTED FLUID SUNSCREEN BROAD SPECTRUM SPF 40 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63730-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE78 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION250 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
C15-19 ALKANE (UNII: CI87N1IM01)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
NIACINAMIDE (UNII: 25X51I8RD4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
COCO-CAPRYLATE (UNII: 4828G836N6)  
PROPANEDIOL (UNII: 5965N8W85T)  
PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ARGININE (UNII: 94ZLA3W45F)  
TOCOPHEROL (UNII: R0ZB2556P8)  
LYSINE (UNII: K3Z4F929H6)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
POLYGLYCERIN-6 (UNII: M51422LRAM)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63730-001-014 mL in 1 PACKET; Type 0: Not a Combination Product06/01/2021
2NDC:63730-001-021 in 1 BOX06/01/2021
210 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:63730-001-031 in 1 BOX06/01/2021
330 mL in 1 TUBE; Type 0: Not a Combination Product
4NDC:63730-001-041 in 1 BOX06/01/2021
430 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/01/2021
Labeler - NATURA BISSE INTERNATIONAL SA (464431576)

Revised: 10/2023
Document Id: 08aaf4ce-9b1b-5491-e063-6294a90a8a4e
Set id: bf8b71c7-257b-0eb6-e053-2a95a90a3a4c
Version: 4
Effective Time: 20231026
 
NATURA BISSE INTERNATIONAL SA