Alcare Antiseptic Handrub Liquid
FDA Label NDC 11084-035

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sc Johnson Professional Usa, Inc. for the product Alcare Antiseptic Handrub (NDC 11084-035). 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 other, active ingredient, purpose, uses, warnings, when using this product, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredient

Ethyl Alcohol, 70% v/v

Purpose

Antibacterial

Uses

  • for hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

Flammable: Keep away from fire or flame.

When Using This Product

  • avoid contact with eyes. In case of eye contact, flush with water

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.

Directions

  • apply sanitizer to cover hands
  • rub into skin
  • no rinsing required

Inactive Ingredients

aqua (water), glycerin, hydroxypropyl cellulose, panthenol, parfum (fragrance), trisodium dicarboxymethyl alaninate.

Principal Display Panel - 1 Liter Bottle Label

SCJ PROFESSIONAL
HEALTHCARE

Alcare®

NDC 11084-035-27

Antiseptic Handrub Liquid

Excellent Moisturization

Net Contents: 1 Liter (33.8 fl oz)
SAP # 4000009648

REORDER #
ALCELV100
L-1448 RO

deb
SKIN CARE

Principal Display Panel (1 Liter Bottle Label)

Principal Display Panel (1 Liter Bottle Label)

* Please review the disclaimer below.