Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32 by Allure Labs Inc DRUG FACTS

Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32 by

Drug Labeling and Warnings

Daily SPF Facial SunscreenLotion Broad Spectrum SPF 32 by is a Otc medication manufactured, distributed, or labeled by Allure Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DAILY SPF FACIAL SUNSCREENLOTION BROAD SPECTRUM SPF 32- zinc oxide cream 
Allure Labs Inc

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.

----------

DRUG FACTS

Active Ingredients:

Zinc Oxide 21%

Purpose: Sunscreen

Uses:

• Helps prevent sunburn. If used as directed with other sun protection measures (see Direction), decreases the risk of skin cancer and early skin aging caused by the sun.

Warning: For external use only.

Do not use: on damaged or broken skin.

When using this products: 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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Apply generously 15 minutes before sun exposer. Reapply at least every 2 hours. Use a water resistant sunscreen if swimming or sweating. 

Sun protection measures: Spending time in the sun increase 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 10am - 2pm.
• Wear long sleeved shirts, pants, hats and sunglasses.

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

Inactive Ingredients: Water (Aqua), Caprylyc/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Tocopheryl Acetate, Helianthus annuus (sunflower) seed oil, Coco-Glucoside, Glyceryl Caprylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Glucoside, Xanthan Gum, Coco-Caprylate/Caprate, Lecithin, Caprylyl/Capryl Glucoside, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Oryza Sativa Starch, Dipotassium Glycyrrhizate, Bisabolol, Caprylhydroxamic Acid, Sodium Pthalate, Sclerotium Gum, Sucrose, Phaeodactylum Tricornutum Extract, Glucose, Spirulina Maxima Extract, Tocopherol, C10 Alochol, C8 Alcohol. 

Distributed by 

Onekind.25 Inc

San Francisco, CA 94107 USA

www.cocokind.com

DAILY SPF FACIAL SUNSCREENLOTION BROAD SPECTRUM SPF 32 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4192
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	210 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
COCONUT ALKANES (UNII: 1E5KJY107T)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARGAN OIL (UNII: 4V59G5UW9X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCO GLUCOSIDE (UNII: ICS790225B)
SUNFLOWER OIL (UNII: 3W1JG795YI)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
SHEA BUTTER (UNII: K49155WL9Y)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
XANTHAN GUM (UNII: TTV12P4NEE)
STARCH, RICE (UNII: 4DGK8B7I3S)
ISOSTEARIC ACID (UNII: X33R8U0062)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
LEVOMENOL (UNII: 24WE03BX2T)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PHYTATE SODIUM (UNII: 88496G1ERL)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
SUCROSE (UNII: C151H8M554)
PHAEODACTYLUM TRICORNUTUM (UNII: Y5W63E7HLV)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
SPIRULINA MAXIMA (UNII: 9K7IG15M0Q)
TOCOPHEROL (UNII: R0ZB2556P8)
C8-10 ALCOHOLS (UNII: 6X61I5U3A4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4192-2	1 in 1 CARTON	11/03/2020
1	NDC: 62742-4192-1	48 g 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 final	part352	11/03/2020

Labeler - Allure Labs Inc (926831603)

Revised: 11/2020

Document Id: a09f6a61-08e1-4e5c-9562-cf6eb866e85b

34390-5

Set id: a8d172a4-d11f-4b3f-a407-1f08dfd0a158

Version: 1

Effective Time: 20201102