Clenova Gel Hand Sanitizer 70% Alcohol

Clenova Gel Hand Sanitizer by

Drug Labeling and Warnings

Clenova Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Pantero, Frestedt Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CLENOVA GEL HAND SANITIZER- 70% alcohol gel 
Pantero

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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Clenova Gel Hand Sanitizer 70% Alcohol

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that can potentially 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.

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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)
• May discolor some fabrics
• May damage wood finishes or plastics

Inactive ingredients

Fragrance, Glycerin, Isopropyl Alcohol, PEG-6 (and) AMP-Acrylates/Vinyl Isodecaoate Crosspolymer, Purified Water USP

Package Label - Principal Display Panel

3785 mL NDC: 74153-382-01

59 mL NDC: 74153-382-02

118 mL NDC: 74153-382-04

5000 mL NDC: 74153-382-05

237 mL NDC: 74153-382-08

473 mL NDC: 74153-382-16

946 mL NDC: 74153-382-32

CLENOVA GEL HAND SANITIZER 
70% alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74153-382(NDC: 74153-380)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
RAPIDGEL EZ1 (UNII: 33JH4A7R2K)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74153-382-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
2	NDC: 74153-382-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
3	NDC: 74153-382-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
4	NDC: 74153-382-05	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
5	NDC: 74153-382-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
6	NDC: 74153-382-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020
7	NDC: 74153-382-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2020	09/10/2021

Labeler - Pantero (116669041)

Registrant - Frestedt Inc. (018853696)

Establishment
Name	Address	ID/FEI	Business Operations
Pantero		116669041	pack(74153-382) , label(74153-382) , manufacture(74153-382) , repack(74153-382) , relabel(74153-382)

Revised: 9/2021

Document Id: cbab2b59-692c-4409-e053-2a95a90abb1b

34390-5

Set id: af7a4115-41d6-5c77-e053-2995a90aeb34

Version: 2

Effective Time: 20210910