NEUTREVO ALCOHOL WET WIPES- alcohol, hydrogen peroxide cloth

Neutrevo Alcohol Wet Wipes by

Drug Labeling and Warnings

Neutrevo Alcohol Wet Wipes by is a Otc medication manufactured, distributed, or labeled by SCK ZETA DIS TICARET. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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) (70%, 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 .
3. Hydrogen peroxide (0.125% v/v).
4. Triethanolamine
5. 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: Antibacterial

Hydrogen Peroxide 0.125 v/v Purpose: Antibacterial

Purpose

Antibacterial - Antiseptic

Use

Alcohol wet wipe to help reduce bacteria on the skin.

Warnings

For external use only. Before using certainly read the label and the instructions. Avoid direct contact with eyes. Flammable liquid and vapour. Keep away from heat , hot surfaces, sparks, open-ames and other ignition sources. No smoking. Keep container tightly closed. Use only non-sparking tools. Store in a well ventilated place. Keep cool

Do not use

• on open skin wounds

WHEN USING

When using this product Keep out of reach of children, food and animal feeds. Do not eat, dirnk and smoking. Follow use instructions to prevent risks on human and environmental health.If contact the skin: This product is produced to contact the skin. Wash the excess with water. In case of redness, swelling, itching or burning occurs, get medical help.In case of eye contact: wash the eyes with the clean water at least 15 minutes with the eyes cover open. If swallowed shake the mouth with water. Do not induce vomiting. Immediately apply to the doctor and show him the label of the product.

STOP USE

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Use wipes as much as needed, used by wiping the hands, between the fingers, all internal and external surfaces and under the nails. Do not rinse after use.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 30C (86F)

Inactive ingredients

glycerin, triethanolamin, water

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

NEUTREVO ALCOHOL WET WIPES 
alcohol, hydrogen peroxide cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 86818-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	0.125 mL  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 86818-005-02	120 in 1 PACKAGE	03/30/2020
1	NDC: 86818-005-01	3.04 mL in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 86818-005-04	100 in 1 PACKAGE	03/30/2020
2	NDC: 86818-005-03	3.04 mL in 1 PATCH; Type 0: Not a Combination Product
3	NDC: 86818-005-06	80 in 1 PACKAGE	03/30/2020
3	NDC: 86818-005-05	3.04 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - SCK ZETA DIS TICARET (356290986)

Registrant - SCK ZETA DIS TICARET (356290986)

Establishment
Name	Address	ID/FEI	Business Operations
SCK ZETA DIS TICARET		356290986	manufacture(86818-005)