Luminess SPF30 Sunscreen Setting Powder 3 Pack

Luminess SPF 30 sunscreen setting powder by

Drug Labeling and Warnings

Luminess SPF 30 sunscreen setting powder by is a Otc medication manufactured, distributed, or labeled by Kinetics Derma Beauty, L.L.C. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LUMINESS SPF 30 SUNSCREEN SETTING POWDER- zinc oxide,titanium dioxide powder 
Kinetics Derma Beauty, L.L.C

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Luminess SPF30 Sunscreen Setting Powder 3 Pack

Luminess SPF 30 Inactive Ingredients

Luminess SPF 30 Inactive Ingredients

Luminess SPF 30 active Ingredients

Luminess SPF active Ingredients

Luminess SPF 30 Dosage and administration

Luminess SPF 30 Dosage and administration

Luminess SPF 30 Keep out of reach of children

Luminess SPF 30 Keep out of reach of children

Luminess SPF 30 Purpose

Luminess SPF 30 Purpose

Luminess SPF 30 Usage

Luminess SPF  30 uses

Luminess SPF 30 Warnings

Luminess SPF 30 warnings

Luminess SPF 30 Instructions for Use

Luminess SPF 30 Instructions for use

Luminess SPF 30 Principle Display panel

Lumiess SPF Front panel

LUMINESS SPF 30 SUNSCREEN SETTING POWDER 
zinc oxide,titanium dioxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73368-105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.012 g  in 0.15 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.0375 g  in 0.15 g
Inactive Ingredients
Ingredient NameStrength
BORON NITRIDE (UNII: 2U4T60A6YD)  
MICA (UNII: V8A1AW0880)  
THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)  
POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)  
MAGNESIUM MYRISTATE (UNII: Z1917F0578)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73368-105-033 g in 1 CELLO PACK; Type 0: Not a Combination Product03/26/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35203/26/202101/10/2023
Labeler - Kinetics Derma Beauty, L.L.C (117146776)
Registrant - Kinetics Derma Beauty, L.L.C (117146776)
Establishment
NameAddressID/FEIBusiness Operations
Kinetics Derma Beauty, L.L.C117146776manufacture(73368-105)

Revised: 1/2023