HAND SANITIZER- alcohol liquid 
Buck Baits, 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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Hand Sanitizer

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 80% 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

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

Other information

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

118mL NDC: 77724-001-01

Buck Baits 118 ml Front Label Sprayer

118 mL NDC: 77724-001-01

Buck Baits Back Label 118ml Sprayer

118 ML NDC: 77724-002-01

Buck Baits Front Label 118ml Sprayer

118 ml NDC: 77724-002-01

Buck Baits 118 ml Sprayer Back

118 ml NDC: 77724-002-02

Buck Baits Front 118ml Bottle w cap

118 ml NDC: 77724-002-02

Buck Baits118 ml Back bottle w cap

3785 ml NDC: 77724-002-03

Buck Baits Front Back Label 3785ml Jug

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77724-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL79.36 mL  in 80 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL3.96 mL  in 80 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 80 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 4.18 mL  in 80 mL
WATER (UNII: 059QF0KO0R) 11.05 mL  in 80 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77724-002-011 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/13/2020
2NDC:77724-002-021 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/13/2020
3NDC:77724-002-031 mL in 1 JUG; Type 0: Not a Combination Product05/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/13/2020
HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77724-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL79.36 mL  in 80 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL3.96 mL  in 80 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 80 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 4.18 mL  in 80 mL
WATER (UNII: 059QF0KO0R) 11.05 mL  in 80 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77724-001-011 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/13/2020
Labeler - Buck Baits, LLC (080413314)
Establishment
NameAddressID/FEIBusiness Operations
Buck Baits LLC080413314manufacture(77724-001) , relabel(77724-002)

Revised: 5/2020
Document Id: a5775191-844f-7acc-e053-2995a90acae1
Set id: a5775c95-76f6-3f13-e053-2a95a90afab5
Version: 1
Effective Time: 20200512
 
Buck Baits, LLC