Jianerkang Wipes

Manufacturer: Jianerkang Medical Co., Ltd
Effective date: 2023-10-23
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:57:20

Label at a glance#

ProductJianerkang Wipes

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Apply wipe thoroughly onto hands and allow to dry. No rinsing required. Discard after single use. Dispose if used wpes in trash receptacle. Don not flush. If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, sanitize with a second wipe. When not in use, keep lid closed to prevent evaporation.

Contacts and useful links#

PhoneLabel contact400-828-2133

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic
For handwashing to decrease bacteria on the skin.
For sanitizing hands after ill persons, or prior to contacting with a person under medical care treatment.
Topical application to skin to help prevent cross-contamination.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire, flame or sources of ignition. i.e. electrocautery procedures.
For external use only.

OTC - DO NOT USE SECTION

Do not use in or contact with eyes.

OTC - STOP USE SECTION

Discontinue use if irritation and redness develop. If condition persists more than 72 hours, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply wipe thoroughly onto hands and allow to dry. No rinsing required.
Discard after single use. Dispose if used wpes in trash receptacle. Don not flush.
If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, sanitize with a second wipe.
When not in use, keep lid closed to prevent evaporation.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

OTC - QUESTIONS SECTION

Questions? Call 400-828-2133

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1307051	ethanol 75 % Medicated Pad	PSN	3
1307051	ethanol 0.75 ML/ML Medicated Pad	SCD	3
1307051	ethanol 75 % Hand Sanitizer Wipes	SY	3
1307051	ethyl alcohol 75 % Topical Cloth	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
34645-0004-1	Jianerkang Wipes	10.466 mL in 1 POUCH	CLOTH	10.466		3
34645-0004-1	Jianerkang Wipes	50 in 1 BAG	CLOTH	50		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
34645-0004	JIANERKANG WIPES (ALCOHOL) CLOTH [JIANERKANG MEDICAL CO., LTD]	3	Current NDC, Legacy NDC, 2 package rows	20231023_a49afe9a-3eaa-401b-e053-2995a90a9245.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Jianerkang Wipes
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
34645-0004	34645-0004-1

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Jianerkang Wipes	ALCOHOL	Jianerkang Medical Co., Ltd	a49afe9a-3eaa-401b-e053-2995a90a9245	2023-10-23	Warnings	Exact identifier ndc (package): 34645-0004-1 ndc (product): 34645-0004 ndc11 (package): 34645000401 spl id: 085ce1b9-2652-8067-e063-6294a90afc04 spl set id: a49afe9a-3eaa-401b-e053-2995a90a9245

Reported adverse events (FAERS/openFDA)#

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