PROJECT REEF MINERAL SUNSCREEN SPF-50- zinc oxide, titanium dioxide lotion 
Project Reef LLC

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PROJECT REEF Mineral Sunscreen SPF-50

Drug Facts

Active Ingredients

Zinc Oxide 14.00 %  Titanium Dioxide 6.00 %

Purpose

Sunscreen

Uses:

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

Warnings:

not intended for ingestion. 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:

• Apply liberally 15 minutes before sun exposure • Children under 6 months of age: ask a doctor. • Reapply at least every 2 hours • Reapply as needed or after towel drying, swimming, or sweating. • Use a water-resistant sunscreen if swimming or sweating • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with 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-sleeved shirts, pants, hats, and sunglasses






Sun Protection Measures.

Other Information:

• Protect the product in this container from excessive heat and direct sun.

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, Lavandula Angustifolia (Lavender) Oil, Polyhydroxystearic Acid, *Punica Granatum (Pomegranate) Extract, Rubus Idaeus (Raspberry) Extract, Stearic Acid, Tridecyl Salicylate, Xanthan Gum, Zemea (Corn) Propanediol. *Denotes Organic Ingredient

Questions?

Call 800 914 0146

Package Labeling:

Label02

PROJECT REEF MINERAL SUNSCREEN SPF-50 
zinc oxide, titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81637-299
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
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE60 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, COLD PRESSED (UNII: AKN3KSD11B)  
COCONUT OIL (UNII: Q9L0O73W7L)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
ETHYL VANILLIN (UNII: YC9ST449YJ)  
FUCUS VESICULOSUS (UNII: 535G2ABX9M)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)  
RASPBERRY (UNII: 4N14V5R27W)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CORN (UNII: 0N8672707O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81637-299-00946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product03/21/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02003/21/2022
Labeler - Project Reef LLC (096500461)

Revised: 11/2023
Document Id: 09e285b2-b615-08b4-e063-6394a90a8964
Set id: 87b9170c-956e-4aa2-9416-da00cca81b58
Version: 2
Effective Time: 20231111
 
Project Reef LLC