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Foaming hand - Medication Information

Product NDC Code 41366-056
Drug Name

Foaming hand

Type Brand
Active Ingredients
Cocoyl methyl monoethanolamine 1.2 g/100ml
Lauramidopropyl betaine 5 g/100ml
Route EXTRACORPOREAL
Dosage Form LIQUID
Labeler Name Zhejiang Meimi Technology Co., Ltd.
Packages
Package NDC Code Description
41366-056-01 259 ml in 1 bottle (41366-056-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient(s) Sodium Laureth Sulfate, Cocamide Methyl MEA.

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
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.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Purpose

Information about the drug product’s indications for use.
Antimicrobial

Spl product data elements

Usually a list of ingredients in a drug product.
Foaming Hand Foaming Hand Soap POLYOXYL 40 HYDROGENATED CASTOR OIL ALOE VERA LEAF SODIUM BENZOATE ETHYLHEXYLGLYCERIN D&C RED NO. 33 COCOYL METHYL MONOETHANOLAMINE COCOYL METHYL MONOETHANOLAMINE WATER SODIUM LAURETH SULFATE PHENOXYETHANOL GLYCERIN POTASSIUM SORBATE ACONITIC ACID EDETATE DISODIUM ANHYDROUS FD&C BLUE NO. 1 LAVANDULA X INTERMEDIA FLOWER LAURAMIDOPROPYL BETAINE LAURAMIDOPROPYL BETAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Label - Principal Display Panel 259 mL in 1 BOTTLE NDC: 41366-056-01 259ml label

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES. IF THIS OCCURS, RINSE THOROUGELY WITH WATER. KEEP OUT OF REACH OF CHILDREN.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API