Hand Sanitizer by Siebert Inc Hand Sanitizer

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Siebert Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- isopropyl alcohol gel 
Siebert Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Sanitizer

Active Ingredient(s)

Isopropyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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.

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, purified water USP, hydroxypropyl methylcellulose

Package Label - Principal Display Panel

59 ml NDC: 76835-002-01

HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76835-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76835-002-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/05/2020
2	NDC: 76835-002-02	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/04/2020
3	NDC: 76835-002-03	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/04/2020
4	NDC: 76835-002-04	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/04/2020
5	NDC: 76835-002-05	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/04/2020
6	NDC: 76835-002-06	18927 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/04/2020
7	NDC: 76835-002-07	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Siebert Inc (058590134)

Establishment
Name	Address	ID/FEI	Business Operations
Siebert Inc		058590134	manufacture(76835-002)

Revised: 1/2023

Document Id: f1f01b41-eeb5-09b1-e053-2a95a90a1c40

34390-5

Set id: a75c9d25-3c21-3034-e053-2a95a90a2511

Version: 6

Effective Time: 20230110