FDA.reportPublic FDA data

Nuvik Alcohol Wipes

Manufacturer
Nuvik Usa, Inc.
Effective date
2023-08-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:26:48

Label at a glance#

ProductNuvik Alcohol Wipes
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

 adults and children 2 years and over  ■ apply to hands  ■ allow to dry without wiping children under 2 years  ■ ask a doctor before use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Use decreases bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Do not useif you are allergic to any of the ingredients

When using this productdo not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctorif irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

 adults and children
2 years and over 		 ■ apply to hands
 ■ allow to dry without wiping
children under 2 years ■ ask a doctor before use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

2-Bromo-2-Nitropropane-1,3-Diol, Aloe Vera, Aqua (Water), Disodium cocoamphodiacetate, Fragrance, Glycerin, PEG 40 Hydrogenated Castor Oil, Phenoxyethanol, Propylene Glycol

Questions or Comments?

OTC - QUESTIONS SECTION

call (855) 55-CLOTH; (1-855-552-5684), M-F

SPL UNCLASSIFIED SECTION

Crocodile Cloth ®| www.crocodilecloth.com

Recyclable packaging

Safe on skin and most surfaces

Store between 40-75°F

Do not flush used wipes

Manufactured for:

Nuvik USA Inc

Columbus, Ohio, USA

Tel: +1(855) 55-CLOTH

www.nuvikglobal.com

Made in Vietnam

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74602-775-802023-08-28C16284748780-1d6a99b39-4514-a426-e053-dadaa90af4c2nuvik 75% Alcohol WIPES
74602-775-802023-07-28C16284748780-1d6a99b39-4514-a426-e053-dadaa90af4c2nuvik 75% Alcohol WIPES
74602-775-802022-02-15C16284748780-1d6a99b39-4514-a426-e053-dadaa90af4c2nuvik 75% Alcohol WIPES
74602-775-802022-01-28C16284748780-1d6a99b39-4514-a426-e053-dadaa90af4c2nuvik 75% Alcohol WIPES

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74602-77574602-775-80

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BRONOPOL6PU1E16C9WIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
GLYCERINPDC6A3C0OXIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
03fe2996-66e2-5973-e063-6294a90a5b95c4a5fe86-1b7f-4388-b259-bc385a78f08f2023-08-28WarningsExact identifier
spl id: 03fe2996-66e2-5973-e063-6294a90a5b95
spl set id: c4a5fe86-1b7f-4388-b259-bc385a78f08f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.