FDA.reportPublic FDA data

NTS Alcohol Wipes

Manufacturer
Nano Technology Solutions
Effective date
2020-06-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:36

Label at a glance#

ProductNTS Alcohol Wipes
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information store between 15-30°C (59-86°F) avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 75%

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

helps reduce bacteria on the skin that can potentially cause disease

WARNINGS SECTION

Warnings
For external use only.
Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last 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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • remove wipe from package and rub thoroughly over all surfaces of both hands
  • rub hands together until dry
  • supervise children under 6 years old
  • not recommended for infants

STORAGE AND HANDLING SECTION

Other information

  • store between 15-30°C (59-86°F)
  • avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive ingredient water

SPL UNCLASSIFIED SECTION

Distributed by Nano Technology Solutions

1212 Maple Drive, Suite B

Troy, MI 48083

(248) 234-4201

Made in China

nano-technologysolutions.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Wipes
Alcohol 75%
Antiseptic Wipes
50 Wipes

NTS Wipe PDP FinalNTS Wipe PDP Final

NTS Wipe Back FinalNTS Wipe Back Final

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76537-004-502022-01-28C16284748780-1d6a99b39-c1ad-a426-e053-dadaa90af4c2NTS Alcohol Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76537-004-50NTS Alcohol Wipes50 in 1 PACKAGECLOTH501
76537-004-50NTS Alcohol Wipes4.7 mL in 1 APPLICATORCLOTH4.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76537-004NTS ALCOHOL WIPES (ETHANOL) CLOTH [NANO TECHNOLOGY SOLUTIONS]1Legacy NDC, 2 package rows20200609_a7811e98-1a19-024b-e053-2995a90aa622.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76537-00476537-004-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
a7811e98-1a1a-024b-e053-2995a90aa622a7811e98-1a19-024b-e053-2995a90aa6222020-06-07WarningsExact identifier
spl id: a7811e98-1a1a-024b-e053-2995a90aa622
spl set id: a7811e98-1a19-024b-e053-2995a90aa622

Reported adverse events (FAERS/openFDA)#

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