Ohui Sun Science Sun Block Ex Plus Beige
FDA Label NDC 53208-524

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 Sun Science Sun Block Ex Plus Beige (NDC 53208-524). 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, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

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

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.

Package Label.Principal Display Panel

OH Sun Science Powder Sun Block EX plus_Beige

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