Active Ingredient(S)
Sodium Laureth Sulfate, Cocamide Methyl MEA.
Foaming Hand Liquid
FDA Label NDC 41366-056
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Meimi Technology Co., Ltd. for the product Foaming Hand (NDC 41366-056). 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 active ingredient(s), warnings, otc - keep out of reach of children, directions, inactive ingredients, otc - purpose, indications & usage, 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
- FOR EXTERNAL USE ONLY.
- AVOID CONTACT WITH EYES. IF THIS OCCURS, RINSE THOROUGELY WITH WATER.
- KEEP OUT OF REACH OF CHILDREN.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.
Inactive Ingredients
WATER, LAURAMIDOPROPL BETAINE, GLYCERIN, PHENOXYETHANOL, POTASSIUM SORBATE, FRAGRANCE, SODIUM
BENZOATE, PEG-40 HYDROGENATED CASTOR OIL, ETHYLHEXYLGLYCERIN, ALOE BARBADENSIS LEAF EXTRACT, CITRIC ACID, DISODIUM EDTA, BLUE 1, RED 33.
Otc - Purpose
Antimicrobial
Indications & Usage
APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.
Package Label - Principal Display Panel
259 mL in 1 BOTTLE
NDC: 41366-056-01
259ml Label (259ml 1)
* Please review the disclaimer below.
