Modesa
FDA Label NDC 58194-005

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shanghai Weierya Daily Chemicals Factory for the product Modesa (NDC 58194-005). 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 inactive ingredient, otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, dosage & administration, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Inactive Ingredient

Inactive Ingredients

carbomer 940, CI 42090, Peg-12 dimethicone, propylene glycol,

tocopheryl acetate, triethanolamine, water

Otc - Active Ingredient

Active Ingredient

Ethyl Alcohol 68% v/v

Otc - Purpose

Purpose

Antimicrobial

Warnings

Warnings

For external use only

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center

right away

Indications & Usage

Uses

hand sanitizer to help reduce bacteria on skin

Dosage & Administration

Directions - Put a dime sized

drop onto hands and rub together briskly

until dry.

Otc - Do Not Use

Do not use in or near the eyes.

In case of contact, rinse eyes thoroughly with water.

Other Safety Information

Flammable. Keep away

from fire or flame

Storage And Handling

Other Information.

Store below 110 F (43C)

Package Label.Principal Display Panel

Copy Of Label (Snowberry Label)

Copy Of Label (Snowberry Label)

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