NDC 53208-524

OHUI Sun Science Sun Block EX plus Beige

Talc, Octinoxate, Zinc Oxide, Titanium Dioxide, Arbutin, Atractylodes Japonica Root Oil

OHUI Sun Science Sun Block EX plus Beige is a Topical Powder in the Human Otc Drug category. It is labeled and distributed by Lg Household And Healthcare, Inc.. The primary component is Talc; Octinoxate; Zinc Oxide; Titanium Dioxide; Arbutin; Atractylodes Japonica Root Oil.

Product ID53208-524_ac4cc8c4-fa77-431c-b13a-02b424572f06
NDC53208-524
Product TypeHuman Otc Drug
Proprietary NameOHUI Sun Science Sun Block EX plus Beige
Generic NameTalc, Octinoxate, Zinc Oxide, Titanium Dioxide, Arbutin, Atractylodes Japonica Root Oil
Dosage FormPowder
Route of AdministrationTOPICAL
Marketing Start Date2011-05-25
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameLG Household and Healthcare, Inc.
Substance NameTALC; OCTINOXATE; ZINC OXIDE; TITANIUM DIOXIDE; ARBUTIN; ATRACTYLODES JAPONICA ROOT OIL
Active Ingredient Strength55 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 53208-524-02

1 CONTAINER in 1 BOX (53208-524-02) > 20 g in 1 CONTAINER (53208-524-01)
Marketing Start Date2011-05-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53208-524-01 [53208052401]

OHUI Sun Science Sun Block EX plus Beige POWDER
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-25

NDC 53208-524-02 [53208052402]

OHUI Sun Science Sun Block EX plus Beige POWDER
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-25
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
TALC55.493 g/100g

OpenFDA Data

SPL SET ID:f2c7c787-92eb-4ba6-9cb2-db4e5306a5d7
Manufacturer
UNII

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