HAND SANITIZER- alcohol gel 
Alpha Pack Ltd

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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Prudence Hand Sanitizer 72% 1000 mL

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 72% 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

Propylene glycol, purified water USP, Triethanolamine, PEG-75 Lanolin, Fragrance

Package Label - Principal Display Panel

Label 1000 ml 72per

DFT 236mL

1000 mL NDC: 78649-010-01

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78649-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL720 mL  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER 940 (UNII: 4Q93RCW27E) 3 mL  in 1000 mL
PEG-75 LANOLIN (UNII: 09179OX7TB) 5 mL  in 1000 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 10 mL  in 1000 mL
WATER (UNII: 059QF0KO0R) 261.7 mL  in 1000 mL
TROLAMINE (UNII: 9O3K93S3TK) 0.3 mL  in 1000 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78649-010-011000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/05/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/05/2020
Labeler - Alpha Pack Ltd (204135164)
Registrant - Alpha Pack Ltd (204135164)
Establishment
NameAddressID/FEIBusiness Operations
SEKTOR KIMYA DETERJAN SANAYI VE TICARET ANONIM SIRKETI533132559manufacture(78649-010)

Revised: 12/2020
Document Id: b621bd24-240f-4daf-e053-2995a90a9df5
Set id: a8b5d0d2-b28d-3be1-e053-2a95a90a95de
Version: 2
Effective Time: 20201210
 
Alpha Pack Ltd