Drugplain

Foaming Hand 1.2 g/100mL

Foaming Hand Soap · LIQUID · Zhejiang Meimi Technology Co., Ltd.

10 Recalls on Record
Plain English

Foaming Hand is a liquid containing foaming hand soap at 1.2 g/100mL, taken extracorporeal. Manufactured by Zhejiang Meimi Technology Co., Ltd..

Key Facts

Brand Name
Foaming Hand
Generic Name
Foaming Hand Soap
NDC Code (Product)
41366-056
Manufacturer
Zhejiang Meimi Technology Co., Ltd.
Strength
1.2 g/100mL
Dosage Form
LIQUID
Route
EXTRACORPOREAL
Marketing Status
Marketing Start
04/18/2022

Recall History

10 Recalls on Record
Class II10/26/2018

S.C. Johnson Professional

CGMP Deviations: Product was released to market prior to microbiological testing.

TerminatedVoluntary: Firm initiated
Class II08/23/2017

Inopak Ltd

GMP Deviations; potential bacterial contamination may have been introduced to products through a contaminated diaphragm pump

TerminatedVoluntary: Firm initiated
Class II08/15/2022

Ultra Chem Labs Corp

Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.

TerminatedN/A
Class II02/19/2024

Seatex LLC

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

TerminatedVoluntary: Firm initiated
Class II05/16/2023

Alpha Aromatics

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

TerminatedVoluntary: Firm initiated
Class II02/19/2024

Seatex LLC

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

TerminatedVoluntary: Firm initiated
Class II07/15/2022

Aire-Master of America Inc

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

TerminatedVoluntary: Firm initiated
Class II09/17/2012

DermaCare, Inc.

Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification.

TerminatedVoluntary: Firm initiated
Class II07/15/2022

Aire-Master of America Inc

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

TerminatedVoluntary: Firm initiated
Class II09/17/2012

DermaCare, Inc.

Microbial Contamination of Non-Sterile Products: Laboratory findings of high total plate count above specification.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

toxicity to various agents5,963 reports
completed suicide5,412 reports
drug abuse5,273 reports
death2,205 reports
fatigue2,134 reports
overdose2,024 reports
confusional state1,839 reports
pain1,819 reports
vomiting1,793 reports
rash1,785 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use

Dosage & Administration

Directions Dispense an adequate amount of hand sanitizer Rub hands together until completely dry

Warnings

Warnings Flammable. Keep away from fire or flame. For external use only. When using this product do not use in or near eyes. If in eyes, flush thoroughly with water. If irritation or rash appears and persists, stop use and see a physician. Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Adverse Reactions

If irritation or rash appears and persists, stop use and see a physician.

Frequently Asked Questions

What is Foaming Hand used for?

Foaming Hand contains Foaming Hand Soap. It is a liquid taken extracorporeal. Consult your doctor for specific uses.

Is Foaming Hand a controlled substance?

Foaming Hand is not classified as a controlled substance by the DEA.

What is the generic name for Foaming Hand?

The generic name for Foaming Hand is Foaming Hand Soap. There are no other listed brand versions of Foaming Hand Soap.

What is the NDC code for Foaming Hand 1.2 g/100mL?

The NDC (National Drug Code) for Foaming Hand 1.2 g/100mL is 41366-056, listed by Zhejiang Meimi Technology Co., Ltd..

Product NDC

41366-056

Package NDC

41366-056-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)