Hand Sanitzer by McConnell labs Inc / McConnell Labs Hand Sanitizer

Hand Sanitzer by

Drug Labeling and Warnings

Hand Sanitzer by is a Otc medication manufactured, distributed, or labeled by McConnell labs Inc, McConnell Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITZER- hand sanitizer gel 
McConnell labs 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

Isopropyl Alcohol 70%

Purpose

Antiseptic

Uses

• ​To help reduce bacteria on the skin that potentially can cause disease
• Reccomended for repeated use

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 childen

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)
• Avoud freezing and excessive heat above 40C (104F)

Inactive ingredients

Water (Aqua), Glycerin, Hydroxypropylcellulose, fragrance (parfum)

Questions?

Call us at +1 (541) 526-1417

HAND SANITZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73991-691
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
EUCALYPTUS OIL (UNII: 2R04ONI662)	0.1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27.4 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)	0.4 mL  in 100 mL
PEPPERMINT OIL (UNII: AV092KU4JH)	0.1 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73991-691-08	240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/25/2020
2	NDC: 73991-691-02	59.147 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/25/2020
3	NDC: 73991-691-32	946.352 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/25/2020	08/24/2021

Labeler - McConnell labs Inc (061623240)

Establishment
Name	Address	ID/FEI	Business Operations
McConnell Labs		061623240	manufacture(73991-691)

Revised: 8/2021

Document Id: ca52dfb9-fee7-7b7c-e053-2a95a90ac1f0

34390-5

Set id: b191dad1-e48c-131c-e053-2a95a90a6daf

Version: 4

Effective Time: 20210824