HYDRATING MINERAL SUNSCREEN BS SPF30- zinc oxide cream 
Allure Labs

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Drug Facts

Active ingredient

Zinc Oxide 21%

Purpose: Sunscreen

Use • helps 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 water to remove.

Stop use and ask a doctor if rash occurs

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

Directions • apply liberally 15 minutes before sun exposure •reapply at least every 2 hours • 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 a Broad Spectrum SPF value 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 sun-glasses.

Other information protect this product from excessive heat and direct sun.

CAUTION:

IF YOU HAVE A KNOWN ALLERGY OR EXPERIENCE SENSITIVITY TO ANY OF THE LIST INGREDIENTS, DISCONTINUE USE. FOR EXTERNAL USE ONLY, DO NOT APPLY TO OPEN WOUNDS.

Inactive ingredients: Water (Aqua), Caprylic/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Glyceryl Caprylate, Coco-Glucoside, Tocopheryl Acetate, Helianthus Annuus (Sunflower) Seed Oil, Honey, Avena sativa (Oat) Kernel Flour, Sodium Phytate, Caprylyl/Capryl Glucoside, Xanthan Gum, Dipotassium Glycyrrhizate, Sclerotium Gum, Cetearyl Glucoside, Butyrospermum Parkii (Shea) Butter, Tocopherol, Coco-Caprylate/Caprate, Caprylhydroxamic acid, Sucrose, Spirulina Maxima Extract, Phaeodactylum Tricornutum Extract, Oryza Sativa Starch, Bisabolol,Lecithin, Polyhydroxystearic acid, Polyglyceryl-3 Polyricinoleate, Isostearic acid, Beta-Sitosterol, Squalene, Glucose, C8 Alcohol, C10 Alcohol

Hydrating Mineral Sunscreen BS SPF 30

HYDRATING MINERAL SUNSCREEN BS SPF30 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4260
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE21 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
HONEY (UNII: Y9H1V576FH)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
SQUALENE (UNII: 7QWM220FJH)  
.BETA.-SITOSTEROL (UNII: S347WMO6M4)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
STARCH, RICE (UNII: 4DGK8B7I3S)  
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)  
SPIRULINA MAXIMA (UNII: 9K7IG15M0Q)  
PHAEODACTYLUM TRICORNUTUM (UNII: Y5W63E7HLV)  
DECYL ALCOHOL (UNII: 89V4LX791F)  
COCO GLUCOSIDE (UNII: ICS790225B)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARGAN OIL (UNII: 4V59G5UW9X)  
OATMEAL (UNII: 8PI54V663Y)  
SHEA BUTTER (UNII: K49155WL9Y)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
COCONUT ALKANES (UNII: 1E5KJY107T)  
BETASIZOFIRAN (UNII: 2X51AD1X3T)  
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TOCOPHEROL (UNII: R0ZB2556P8)  
SUCROSE (UNII: C151H8M554)  
LEVOMENOL (UNII: 24WE03BX2T)  
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62742-4260-21 in 1 CARTON04/15/2024
1NDC:62742-4260-148 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/15/2024
Labeler - Allure Labs (926831603)
Registrant - Allure Labs (926831603)
Establishment
NameAddressID/FEIBusiness Operations
Allure Labs926831603manufacture(62742-4260)

Revised: 4/2024
Document Id: 16268c31-2152-20e0-e063-6294a90a7965
Set id: 16268c31-2151-20e0-e063-6294a90a7965
Version: 1
Effective Time: 20240415
 
Allure Labs