Pocket Size Alcohol Formula Hand Sanitizer

Pocket Size Alcohol Formula Hand Sanitizer by

Drug Labeling and Warnings

Pocket Size Alcohol Formula Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

POCKET SIZE ALCOHOL FORMULA HAND SANITIZER- alcohol gel 
Zhejiang iColor Biotech Co., Ltd

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Pocket Size Alcohol Formula Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

• Premium sanitizer to reduce 99.9% of most illness-causing germs and bacteria.
• Antiseptic for hands and skin.
• Sanitize and disinfect hands and skin when water and soap are not available.

Warnings

For external use only

DO NOT INGEST.

Do not use

on open skin or puncture-type wounds. Do not use near or in eyes. If eye contact occurs, flush with cold water. Seek medical attention if irritation persists. Supervise children under 6 years of age when using sanitizer. Stop using if irritation appears. Seek medical attention if irritation persists.

KEEP OUT OF REACH OF CHILDREN.

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

WARNINGS: FLAMMABLE.

Do not use near open flame, fire or spark.

Directions

Clean hands and skin with by placing on hands or skin and gently rubbing No need to rinse, let hands or skin dry

Read all directions and warnings before using Store at room temperature 15° to 34°C (59° to 86° F) with package closed Avoid excessive heat above 40°C (104°F)

Inactive ingredients

Aqua (purified water), acrylates, Aminomethyl propanol, fructose, glycerin, inulin, panthenol, squalene, sodium hyaluronate, tocopheryl acetate

Package Labeling:

POCKET SIZE ALCOHOL FORMULA HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-049
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FRUCTOSE (UNII: 6YSS42VSEV)
GLYCERIN (UNII: PDC6A3C0OX)
INULIN (UNII: JOS53KRJ01)
PANTHENOL (UNII: WV9CM0O67Z)
SQUALENE (UNII: 7QWM220FJH)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-049-01	30 in 1 PACKET	09/07/2020	01/31/2026
1		2 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/07/2020	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)

Revised: 1/2024

Document Id: 0fb3b0fb-a8e6-ab50-e063-6394a90a0397

34390-5

Set id: 85e41d1b-ea5c-4d2c-833d-a314f4be260c

Version: 2

Effective Time: 20240124