PROJECT REEF SPF-30 MINERAL SUNSCREEN- zinc oxide cream 
Project Reef LLC

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PROJECT REEF SPF-30 Mineral Sunscreen

Drug Facts

Active Ingredients

Zinc Oxide 14.00%

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 or irritation develops and lasts.

Keep out of reach of children.

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

If pregnant or breast-feeding,

ask a health professional before use.

Directions:

Other Information:

Inactive Ingredients:

Algae Extract, *Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Benzyl Alcohol, *Butyrospermum Parkii (Shea) Butter, *Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Citric Acid, Citrus Aurantium Dulcis (Orange) Oil, *Cocos Nucifera (Coconut) Oil, Decyl Glucoside, Dehydroacetic Acid, Ethyl Vanillin, Fucus Vesiculosus (Seaweed) Extract, *Glycerin, Glyceryl Stearate, Helianthus Annuus, * Hippophae Rhamnoides (Sea Buckthorn) Oil, Hydroxyethylcellulose, Polyhydroxystearic Acid, *Punica Granatum (Pomegranate) Extract, Rubus Idaeus (Raspberry) Extract, Stearic Acid, Tridecyl Salicylate, Xanthan Gum, Zemea (Corn) Propanediol.

Questions?

Call 800 914 0146

Package Labeling:

New Label

PROJECT REEF SPF-30 MINERAL SUNSCREEN 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81637-139
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION140 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SHEA BUTTER (UNII: K49155WL9Y)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ORANGE OIL (UNII: AKN3KSD11B)  
COCONUT OIL (UNII: Q9L0O73W7L)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
ETHYL VANILLIN (UNII: YC9ST449YJ)  
NORI (UNII: 477TV3P5UX)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
POMEGRANATE (UNII: 56687D1Z4D)  
RUBUS IDAEUS SEED (UNII: M3CL7US2ZG)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CORN (UNII: 0N8672707O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81637-139-00125 mL in 1 TUBE; Type 0: Not a Combination Product03/08/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02003/08/2021
Labeler - Project Reef LLC (096500461)

Revised: 11/2023
Document Id: 09e261d4-ab14-c829-e063-6294a90a8e85
Set id: a6077e6f-d987-4159-946f-3e2397247659
Version: 3
Effective Time: 20231111
 
Project Reef LLC