Alcohol Antibacterial Wipes

Manufacturer
Kunming Ansheng Industry & Trade Co., Ltd.
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:27

Label at a glance#

ProductAlcohol Antibacterial Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

1, Open sticker, pull out the wipe and close sticker tightly. 2, Dispose of used wipes in trash, DO NOT FLUSH.

Storage and handling

Keep in cool dry place, storage temperature: 0-40℃

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v;

Chlorohexidine Diacetate 0.1% v/v;

Benzalkonium 0.1% v/v;

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacterial on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • on infants less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

1, Open sticker, pull out the wipe and close sticker tightly.

2, Dispose of used wipes in trash, DO NOT FLUSH.

Other information

STORAGE AND HANDLING SECTION

Keep in cool dry place, storage temperature: 0-40℃

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Chlorohexidine Diacetate, Benzalkonium Chloride

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 wipes in one bag. NDC: 78183-018-01

50 wipes in one bag. NDC: 78183-018-02

30wipes30wipes

50wipes50wipes

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
78183-018-012022-01-28C16284748780-1d6a99b39-db91-a426-e053-dadaa90af4c2Alcohol Antibacterial Wipes
78183-018-022022-01-28C16284748780-1d6a99b39-db91-a426-e053-dadaa90af4c2Alcohol Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78183-018-01Alcohol Antibacterial Wipes30 U in 1 BAGCLOTH301
78183-018-02Alcohol Antibacterial Wipes50 U in 1 BAGCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78183-018ALCOHOL ANTIBACTERIAL WIPES CLOTH [KUNMING ANSHENG INDUSTRY & TRADE CO., LTD.]1Legacy NDC, 2 package rows20200613_a7da3345-963c-4c1e-e053-2a95a90ac58a.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78183-01878183-018-01, 78183-018-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
a7da3345-962e-4c1e-e053-2a95a90ac58aa7da3345-963c-4c1e-e053-2a95a90ac58a2020-06-11WarningsExact identifier
spl id: a7da3345-962e-4c1e-e053-2a95a90ac58a
spl set id: a7da3345-963c-4c1e-e053-2a95a90ac58a

Reported adverse events (FAERS/openFDA)#

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