Sanimep
FDA Label NDC 79869-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Limep, S.a. De C.v. for the product Sanimep (NDC 79869-000). 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 drug facts, active ingredient(s), purpose, use(s), warnings, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient(S)

Alcohol 80% v/v

Purpose

Antiseptic

Use(S)

Health care personnel hand rub to help reduce bacteria that potentially can cause disease

Warnings

For external use only. Flammable. keep away from heat or flame

Do Not Use

  • in children less than 2 months of age
  • on open skin wounds

When Using This Product

keep out of eyes , ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. 

Stop Use And Ask A Doctor

if irritation or rash occurs. These may be signs of a serious condition. 

Keep Out Of Reach Of Children.

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

glycerin, hydrogen peroxide, purified water USP, mint eucaliptus scent

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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