MAUI VERA REEF FRIENDLY MINERAL SUNSCREEN- zinc oxide lotion 
Maui Vera, Inc.

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Maui Vera Reef Friendly Mineral Sunscreen

Drug Facts

Active ingredient

Zinc Oxide 20%

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 occurs.

Keep out of reach of children.

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

Directions

Other information

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

Inactive ingredients

*Aloe Barbadensis Leaf (Aloe) Juice, *Caprylic/Capric Triglyceride, (Coconut Oil),Cetearyl Olivate, Sorbitane Olivate, Cetearyl Alcohol, Cetyl Alcohol, *Persea Americana (Avocado) Oil, Panthenol (Vitamin B-5), Lauroyl Lysin, Vitamin E Acetate, Polyhydroxy Stearic Acid, Benzyl Alcohol, Dehydroacetic Acid, Xanthan Gum, Sodium Phytate *Organic Ingredients

Questions or comments?

1-415-938-7808

Package Labeling: 89ml

Label

Package Labeling: 192ml

Label2

MAUI VERA REEF FRIENDLY MINERAL SUNSCREEN 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81409-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
AVOCADO (UNII: SDS87L369F)  
PANTHENOL (UNII: WV9CM0O67Z)  
LAUROYL LYSINE (UNII: 113171Q70B)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81409-001-0189 mL in 1 TUBE; Type 0: Not a Combination Product09/01/2021
2NDC:81409-001-02192 mL in 1 TUBE; Type 0: Not a Combination Product09/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/01/2021
Labeler - Maui Vera, Inc. (019591508)

Revised: 10/2023
Document Id: 08aab616-178b-b096-e063-6394a90a2f88
Set id: ec120bdd-41a8-4e6a-8094-8a5311d99683
Version: 2
Effective Time: 20231026
 
Maui Vera, Inc.