Apothecary Home Hand Sanitizer Spray

Apothecary Home Hand Sanitizer by

Drug Labeling and Warnings

Apothecary Home Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by HOME & BODY COMPANY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

APOTHECARY HOME HAND SANITIZER- alcohol liquid 
HOME & BODY COMPANY

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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Apothecary Home Hand Sanitizer Spray

Active Ingredient(s)

Ethyl Alcohol 80%

Purpose

Antiseptic

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

Water (Aqua)

Package Label - Principal Display Panel

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APOTHECARY HOME HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73746-033
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73746-033-01133 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/04/2020
2NDC: 73746-033-02236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/04/2020
3NDC: 73746-033-03236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/09/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/09/202010/05/2022
Labeler - HOME & BODY COMPANY (081290720)
Registrant - HOME & BODY COMPANY (081290720)
Establishment
NameAddressID/FEIBusiness Operations
HOME & BODY COMPANY081290720manufacture(73746-033)

Revised: 10/2022
Document Id: ea616712-1a8c-1811-e053-2995a90a8fc6
Set id: a7a86bc9-7e3e-0d03-e053-2a95a90ac116
Version: 5
Effective Time: 20221006