OTC Medication Information: OHUI Sun Science Sun Block EX Plus Beige

OHUI SUN SCIENCE SUN BLOCK EX PLUS BEIGE — talc, octinoxate, zinc oxide, titanium dioxide, arbutin and atractylodes japonica root oil powder
LG Household and Healthcare, Inc.

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.

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.

OHUI SUN SCIENCE SUN BLOCK EX PLUS BEIGE talc, octinoxate, zinc oxide, titanium dioxide, arbutin, atractylodes japonica root oil powder

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-524 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TALC (TALC) TALC 55.493 g in 100 g OCTINOXATE (OCTINOXATE) OCTINOXATE 7.2 g in 100 g ZINC OXIDE (ZINC OXIDE) ZINC OXIDE 5.76 g in 100 g TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE 2.59956 g in 100 g ARBUTIN (ARBUTIN) ARBUTIN 2 g in 100 g ATRACTYLODES JAPONICA ROOT OIL (ATRACTYLODES JAPONICA ROOT OIL) ATRACTYLODES JAPONICA ROOT OIL 0.1 g in 100 g

Inactive Ingredients Ingredient Name Strength 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 Code Package Description Multilevel Packaging 1 NDC:53208-524-02 1 CONTAINER (CONTAINER) in 1 BOX contains a CONTAINER (53208-524-01) 1 NDC:53208-524-01 20 g in 1 CONTAINER This package is contained within the BOX (53208-524-02)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/25/2011

Labeler — LG Household and Healthcare, Inc. (688276187)

Registrant — LG Household and Healthcare, Inc. (688276187)

Establishment
Name	Address	ID/FEI	Operations
LG Household and Healthcare, Inc.		688276187	manufacture

Revised: 05/2011 LG Household and Healthcare, Inc.