HAND SANITIZER- alcohol gel 
Whish Body Products

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 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

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

aloe, purified water USP, ispropyl myristate, acrylates/c10-30 acrylates crosspolymer, aminomethylpropandediol, peppermint oil.

Package Label - Principal Display Panel

3.79L Label976mL Label480mL Label390mL Label118 mL Label118 mL NDC: 76224-6822-2

390 mL NDC: 76224-7822-3

488 mL NDC: 76224-7822-4

976 mL NDC: 76224-7822-5

3.79L NDC: 76244-7822-6

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76224-6822
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
MENTHA PIPERITA (UNII: 79M2M2UDA9)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
WATER (UNII: 059QF0KO0R)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76224-6822-5976 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
2NDC:76224-6822-4488 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
3NDC:76224-6822-3390 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
4NDC:76224-6822-2118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
5NDC:76224-6822-63785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2020
Labeler - Whish Body Products (606576952)
Establishment
NameAddressID/FEIBusiness Operations
Whish Body Products606576952manufacture(76224-6822)

Revised: 5/2020
Document Id: a53bb178-5886-0d36-e053-2a95a90aab64
Set id: a53bba4a-70a9-0eee-e053-2a95a90a5ca0
Version: 1
Effective Time: 20200509
 
Whish Body Products