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OHUI Sun Science Sun Block EX plus Beige

Dosage form: powder
Ingredients: TALC 55.493g in 100g, OCTINOXATE 7.2g in 100g, ZINC OXIDE 5.76g in 100g, TITANIUM DIOXIDE 2.59956g in 100g, ARBUTIN 2g in 100g, ATRACTYLODES JAPONICA ROOT OIL 0.1g in 100g
Labeler: LG Household and Healthcare, Inc.
NDC Code: 53208-524

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.

Drug Fact

TALC                        55.493%
OCTINOXATE           7.2% 
ZINC OXIDE              5.76%
TITANIUM DIOXIDE   2.59956%
ARBUTIN                  2%
ATRACTYLODES JAPONICA ROOT OIL  0.1%

For external use only.

Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away

Keep out of eyes. Rinse with water to remove.

OH Sun Science Powder Sun Block EX plus_Beige
OHUI SUN SCIENCE SUN BLOCK EX PLUS BEIGE 
talc, octinoxate, zinc oxide, titanium dioxide, arbutin, atractylodes japonica root oil powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-524
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TALC (TALC) TALC55.493 g  in 100 g
OCTINOXATE (OCTINOXATE) OCTINOXATE7.2 g  in 100 g
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE5.76 g  in 100 g
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE2.59956 g  in 100 g
ARBUTIN (ARBUTIN) ARBUTIN2 g  in 100 g
ATRACTYLODES JAPONICA ROOT OIL (ATRACTYLODES JAPONICA ROOT OIL) ATRACTYLODES JAPONICA ROOT OIL0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALUMINUM HYDROXIDE 
MICA 
DIMETHICONE 
SILICON DIOXIDE 
ALUMINUM STARCH OCTENYLSUCCINATE 
STEARIC ACID 
WATER 
ALCOHOL 
METHYLPARABEN 
FERRIC OXIDE YELLOW 
FERRIC OXIDE RED 
TRIBASIC CALCIUM PHOSPHATE 
FERROSOFERRIC OXIDE 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:53208-524-021 CONTAINER (CONTAINER) in 1 BOX
1NDC:53208-524-0120 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35205/25/2011
Labeler - LG Household and Healthcare, Inc. (688276187)
Registrant - LG Household and Healthcare, Inc. (688276187)
Establishment
NameAddressID/FEIOperations
LG Household and Healthcare, Inc.688276187manufacture

Revised: 05/2011
Document Id: ac4cc8c4-fa77-431c-b13a-02b424572f06
Set id: f2c7c787-92eb-4ba6-9cb2-db4e5306a5d7
Version: 1
Effective Time: 20110525
 
LG Household and Healthcare, Inc.

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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