Anti Bacterial Hand Sanitizer
FDA Label NDC 49852-017

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tri-coastal Design Company Inc. for the product Anti Bacterial Hand Sanitizer (NDC 49852-017). 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, purpose, uses, warnings, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

  • For handwashing to decrease bacteria on the skin

Warnings

  • For external use only
    • Flammable, keep away from fire and flame

      • Does not contain grain alcohol. Do not drink. If taken internally will produce serious gastric disturbances

      Avoid the eyes and mucous membranes.
      In case of contact; rinse area thoroughly with water

Keep Out Of Reach Of Children

If swallowed contact a doctor or Poison Control Center immediately.

Directions

Rub dime sized amount between hands until dry

Other Information

Store below 105F
May discolor some fabrics

Inactive Ingredients

Benzophenone-4, Carbomer, Fragrance, FDC Blue 1, FDC Yellow 5, Glycerin, PEG-40 Hydrogenated Castor Oil, Propylene Glycol, Tocopherol and Jojoba Oil, Triethanolamine, Water (Aqua)

Package Label

Image Of Package Label (Grnhndsntzr)

Image Of Package Label (Grnhndsntzr)


* Please review the disclaimer below.