UV LOCK FLOWER 3 PROOF SUN by NATURE REPUBLIC CO., LTD.

UV LOCK FLOWER 3 PROOF SUN by

Drug Labeling and Warnings

UV LOCK FLOWER 3 PROOF SUN by is a Otc medication manufactured, distributed, or labeled by NATURE REPUBLIC CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UV LOCK FLOWER 3 PROOF SUN SPF50PLUS PA PLUS PLUS PLUS- octinoxate, octisalate, zinc oxide, titanium dioxide cream 
NATURE REPUBLIC CO., LTD.

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.

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ACTIVE INGREDIENT

Active Ingredients: Ethylhexyl Methoxycinnamate 7.5%, Ethylhexyl Salicylate 5%, Zinc Oxide 4.9%, Titanium Dioxide 2.9%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Cyclopentasiloxane, Glycerin, PEG-10 Dimethicone, Dimethicone, Dipropylene Glycol, Magnesium Sulfate, Disteardimonium Hectorite, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone,
Isoamyl p-Methoxycinnamate, Aluminum Hydroxide, Fragrance(Parfum), Stearic Acid, Methylparaben, Chlorphenesin, Caffeine, Butylene Glycol, Propylparaben, Portulaca Oleracea Extract

PURPOSE

Purpose: Sunscreen

WARNINGS

Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

DOSAGE AND ADMINISTRATION

How to Use: Evenly apply an appropriate amount to skin that can be easily exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

UV LOCK FLOWER 3 PROOF SUN  SPF50PLUS PA PLUS PLUS PLUS
octinoxate, octisalate, zinc oxide, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51346-209
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	3.75 mg  in 50 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.5 mg  in 50 mL
Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	2.45 mg  in 50 mL
Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	Titanium Dioxide	1.45 mg  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51346-209-01	50 mL in 1 CARTON; Type 0: Not a Combination Product	02/01/2013	11/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/01/2013	11/01/2019

Labeler - NATURE REPUBLIC CO., LTD. (631172020)

Registrant - NATURE REPUBLIC CO., LTD. (631172020)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(51346-209)

Revised: 2/2020

Document Id: cba74f2c-e728-41da-ae35-23dec7380ebf

34390-5

Set id: 6c6ff12e-369f-4634-9f64-5ee177aed0d8

Version: 2

Effective Time: 20200226

 

NATURE REPUBLIC CO., LTD.