SHEER MINERAL SUNSCREEN BROAD SPECTRUM SPF 30- zinc oxide cream 
Allure Labs

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Drug Facts

Active Ingredients:

Zinc Oxide 18.6%

Purpose: Sunscreen

Uses • helps to prevent sunburn

• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings For external use only

Do not use • on damaged or broken skin.

When using this product • keep out of eyes. Rinse with warm water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If product is swallowed, get medical help, or contact a Poison Control Center right away.

Directions • Apply liberally 15 minutes before sun exposure.

• Children under 6 months: Ask a doctor

• Reapply: at least every 2 hours

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 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-sleeve shirts, pants, hats, and sunglasses.

Other information • Protect this product from excessive heat or direct sun.

Inactive Ingredients:

Water (Aqua),Cyclopentasiloxane, Butylene Glycol, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Cyclohexasiloxane, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Sorbitan Stearate, Dimethicone,Ascorbic Acid, Plankton Extract, Tocopherol, caprylyl Glycol, Caprylic/Capric Triglyceride, Phoenix Dactylifera ( Date) Fruit Extract, Imperata Cylindrica Root Extract, Arabidopsis Thaliana Extract, Ascorbyl Palmitate, Polygonum Aviculare Extract,Tocopheryl Linoleate/Oleate, Teprenone, Xanthan Gum,Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Phenoxyethanol, Ethylhexylglycerin, Hexylene Glycol, PEG-8, Carbomer, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Cetyl Alcohol, Lecithin, Citric Acid, Sodium Lactate, Disodium EDTA, Dipotassium Glycyrrhizate, Micrococcus Lysate.

Sheer Mineral Sunscreen BS SPF 30

SHEER MINERAL SUNSCREEN BROAD SPECTRUM SPF 30 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4242
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE18.6 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)  
TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
DATE (UNII: H3O7QI5HY7)  
POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)  
TEPRENONE (UNII: S8S8451A4O)  
POLYACRYLAMIDE (CROSSLINKED; 2 MOLE PERCENT BISACRYLAMIDE) (UNII: 9FPL31B58Q)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PEG-100 STEARATE (UNII: YD01N1999R)  
TOCOPHEROL (UNII: R0ZB2556P8)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)  
LAURETH-7 (UNII: Z95S6G8201)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM LACTATE, L- (UNII: P2Y1C6M9PS)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LINOLEIC ACID (UNII: 9KJL21T0QJ)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
GLYCERIN (UNII: PDC6A3C0OX)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62742-4242-156.7 g in 1 TUBE; Type 0: Not a Combination Product12/13/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02012/13/2023
Labeler - Allure Labs (926831603)
Registrant - Allure Labs (926831603)
Establishment
NameAddressID/FEIBusiness Operations
Allure Labs926831603manufacture(62742-4242)

Revised: 12/2023
Document Id: 0c6ac094-cb5c-0f09-e063-6394a90a9eed
Set id: 0c6ac094-cb5b-0f09-e063-6394a90a9eed
Version: 1
Effective Time: 20231213
 
Allure Labs