UV LOCK ULTRA MILK SUN SPF50PLUS PA PLUS PLUS PLUS

Dosage form: cream
Ingredients: OCTINOXATE 3.75g in 50mL, ZINC OXIDE 3.25g in 50mL, OCTISALATE 2.50g in 50mL, TITANIUM DIOXIDE 1.25g in 50mL
Labeler: NATURE REPUBLIC CO., LTD.
NDC Code: 51346-042

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.

ACTIVE INGREDIENT

Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.5%, ZINC OXIDE 6.5%, ETHYLHEXYL SALICYLATE 5%, TITANIUM DIOXIDE 2.5%

INACTIVE INGREDIENT

Inactive Ingredients:
WATER, CYCLOPENTASILOXANE, ALCOHOL,BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, ISODECYL NEOPENTANOATE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, PHENOXYETHANOL, CALCIUM ALUMINUM BOROSILICATE, FRAGRANCE, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, SILICA, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, POLYGLYCERYL-6 POLYRICINOLEATE, OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, CELLULOSE GUM, MICROCRYSTALLINE CELLULOSE

PURPOSE

Purpose: Strong milk sun block with daily skincare effects.

WARNINGS


Cautions:
For external use only.
Avoid contact with eyes and mouth.
Discontinue use if signs of irritation or rash 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: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

DOSAGE AND ADMINISTRATION

How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

UV LOCK ULTRA MILK SUN  SPF50PLUS PA PLUS PLUS PLUS
octinoxate, zinc oxide, octisalate, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-042
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE3.75 g  in 50 mL
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE3.25 g  in 50 mL
OCTISALATE (OCTISALATE) OCTISALATE2.50 g  in 50 mL
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE1.25 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CYCLOMETHICONE 5 
ALCOHOL 
BUTYLENE GLYCOL 
DIPROPYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:51346-042-0150 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35201/02/2012
Labeler - NATURE REPUBLIC CO., LTD. (631172020)
Registrant - NATURE REPUBLIC CO., LTD. (631172020)
Establishment
NameAddressID/FEIOperations
NATURE REPUBLIC CO., LTD.631172020manufacture(51346-042)

Revised: 09/2012
 
NATURE REPUBLIC CO., LTD.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web1)