SALISBURY HAND SANITIZER

Salisbury Blending Hand Sanitizer by

Drug Labeling and Warnings

Salisbury Blending Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Salisbury Blending Company, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SALISBURY BLENDING HAND SANITIZER- isopropyl alcohol solution 
Salisbury Blending Company, LLC

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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SALISBURY HAND SANITIZER

DRUG FACTS:

ACTIVE INGREDIENTS: Isopropyl Alcohol 75% v/v

Purpose: Antiseptic

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

WARNINGS: For external use only. Flammable, Keep away from heat or flames.

DO NOT USE:

- in children less than two 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 CONTACT A DOCTOR - if irritation or rash occurs.

These may be a sign of a serious condition.

KEEP OUT OF THE 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 six years of age when using this product to avoid swallowing.

OTHER INFORMATION: Store between 15 - 30 C (59-86 F) Avoid freezing and excessive heat above 40C (104F)

Inactive INGREDIENTS: glycerin, hydrogen peroxide, purified water (USP)

SALISBURY 

BLENDING COMPANY

High Point, NC 27260 (1-800-262-8200)

Isopropyl Alcohol Antiseptic 75%

Topical Solution

Non-sterile Solution

Packaging

IMAGE

SALISBURY BLENDING HAND SANITIZER 
isopropyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79582-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79582-001-10100 mL in 1 BOTTLE; Type 0: Not a Combination Product07/27/202006/15/2021
2NDC: 79582-001-0144 in 1 CASE07/27/202006/15/2021
2NDC: 79582-001-10100 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC: 79582-001-25250 mL in 1 BOTTLE; Type 0: Not a Combination Product07/27/202006/15/2021
4NDC: 79582-001-0244 in 1 CASE07/27/202006/15/2021
4NDC: 79582-001-25250 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC: 79582-001-50500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/27/202006/15/2021
6NDC: 79582-001-033785 mL in 1 BOTTLE; Type 0: Not a Combination Product11/09/202006/15/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/27/202006/15/2021
Labeler - Salisbury Blending Company, LLC (094285171)
Establishment
NameAddressID/FEIBusiness Operations
Salisbury Blending Company, LLC094285171manufacture(79582-001)

Revised: 7/2021
Document Id: 76a40c43-95ed-4e07-a409-3c383e5ff41e
Set id: b57a92ca-10bd-456b-a2e5-bbecb5a888ee
Version: 3
Effective Time: 20210719