FDA.reportPublic FDA data

portable degerming wipe

Manufacturer
Dalian Aikangning Biological Technology Co. LTD
Effective date
2021-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:37

Label at a glance#

Productportable degerming wipe
Active ingredientALCOHOL
Label structure13 sections

Storage and handling

expiration date:24 months Avoid direct sunlight or high temperature

Label contents#

Full prescribing information#

Main materials

OTC - ACTIVE INGREDIENT SECTION

Alcohol, Benzalkonium chloride

SPL UNCLASSIFIED SECTION

Size: 200mm x 150mm Number: 30 pieces

Sanitation standard: GB15979

Executive standard: GB/127728
Saniltation license: Liaoning province health department degerming product certificate No. (2018) B003
Expiration date: 24 months

OTC - PURPOSE SECTION

degerming

usage method

INDICATIONS & USAGE SECTION

  • Open the front sealing paste, and then draw out the wipes for use.
  • Please use it as soon as possible affer opening
  • After opening, please stick the seal well to prevent drying

Attention

WARNINGS SECTION

  • In case of any skin discomfort during use, please stop using immediately and go to the doctor in time
  • Please don't use it in parts with mucous membrane such as eyes or mouth
  • Keep it away from infants.
  • Avoid direct sunlight or high temperature
  • This produdt is water-insoluble non-wovon fabric, can not be directly thrown into the toilet.

OTC - DO NOT USE SECTION

Please don't use it in parts with mucous membrane such as eyes or mouth

OTC - WHEN USING SECTION

degerming

OTC - STOP USE SECTION

In case of any skin discomfort during use, please stop using immediately and go to the doctor in time

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep it away from infants.

DOSAGE & ADMINISTRATION SECTION

Open the front sealing paste, and then draw out the wipes for use.

STORAGE AND HANDLING SECTION

expiration date:24 months

Avoid direct sunlight or high temperature

INACTIVE INGREDIENT SECTION

water, Propylene Glycol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 pcs: 81613-001-01

20 pcs: 81613-001-02

30 pcs: 81613-001-03

60 pcs: 81613-001-04

80 pcs: 81613-001-05

100 pcs: 81613-001-06

120 pcs: 81613-001-07

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81613-001-012022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-022022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-032022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-042022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-052022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-062022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be
81613-001-072022-07-29C16284748780-1e4f33bdf-a995-d8a0-e053-dadaa90a6e4ebc4d65e8-c5f3-b6da-e053-2a95a90a40be

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81613-001-01portable degerming wipe18 mL in 1 BAGCLOTH181
81613-001-02portable degerming wipe36 mL in 1 BAGCLOTH361
81613-001-03portable degerming wipe48 mL in 1 BAGCLOTH481
81613-001-04portable degerming wipe108 mL in 1 BAGCLOTH1081
81613-001-05portable degerming wipe144 mL in 1 BAGCLOTH1441
81613-001-06portable degerming wipe180 mL in 1 BOTTLECLOTH1801
81613-001-07portable degerming wipe216 mL in 1 BOTTLECLOTH2161

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81613-001PORTABLE DEGERMING WIPE (ALCOHOL) CLOTH [DALIAN AIKANGNING BIOLOGICAL TECHNOLOGY CO. LTD]1Legacy NDC, 7 package rows20210228_bc4d65e8-c5f3-b6da-e053-2a95a90a40be.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
81613-00181613-001-01, 81613-001-02, 81613-001-03, 81613-001-04, 81613-001-05, 81613-001-06, 81613-001-07

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT

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
bc4d65e8-c5f4-b6da-e053-2a95a90a40bebc4d65e8-c5f3-b6da-e053-2a95a90a40be2021-02-27WarningsExact identifier
spl id: bc4d65e8-c5f4-b6da-e053-2a95a90a40be
spl set id: bc4d65e8-c5f3-b6da-e053-2a95a90a40be

Reported adverse events (FAERS/openFDA)#

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