Otc - Active Ingredient
TITANIUM DIOXIDE 9.84%OCTINOXATE 4.5%ARBUTIN 2%ATRACTYLODES JAPONICA ROOT OIL 0.1%
Ohui White Extreme Illuminating Pact No.10
FDA Label NDC 53208-534
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lg Household And Healthcare, Inc. for the product Ohui White Extreme Illuminating Pact No.10 (NDC 53208-534). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, warnings and precautions, otc - keep out of reach of children, otc - when using, otc - stop use, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings And Precautions
For external use only
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.
Otc - When Using
Keep out of eyes. Rinse with water to remove
Otc - Stop Use
Stop use if a rash or irritation develops and lasts.
Package Label.Principal Display Panel
OHUI White Extreme Illuminating Pact #20
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