Kenaf wet wipe

Manufacturer: MEDICELL BIO CO., Ltd.
Effective date: 2025-06-24
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:03:50

Label at a glance#

ProductKenaf wet wipe

Active ingredientALLANTOIN

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

INACTIVE INGREDIENT SECTION

Water, etc

OTC - PURPOSE SECTION

Wet tissue

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply to skin and wipe

WARNINGS SECTION

1. For external use only.

1) Do not use over the wound and irritated skin with eczema or infections

2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help

2. Keep the cover closed tight after use

3. Do not put the left over contents back into the container to avoid deterioration

1) Avoid contact with eyes

2) Keep out of reach of children

3) Store in a cool and dry place, away from direct sun light

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72944-0001-1	2025-06-24	C162847	48780-1	e4f33bdf-aecf-d8a0-e053-dadaa90a6e4e	Drug Facts
72944-0001-1	2025-01-30	C162847	48780-1	e4f33bdf-aecf-d8a0-e053-dadaa90a6e4e	Drug Facts
72944-0001-1	2023-02-09	C162847	48780-1	e4f33bdf-aecf-d8a0-e053-dadaa90a6e4e	Drug Facts
72944-0001-1	2022-07-29	C162847	48780-1	e4f33bdf-aecf-d8a0-e053-dadaa90a6e4e	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72944-0001-1	Kenaf wet wipe	190 g in 1 POUCH	LIQUID	190		5

Products#

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

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

Kenaf wet wipe
ALLANTOIN
WATER
1,2-HEXANEDIOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72944-0001	72944-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
1,2-HEXANEDIOL	TR046Y3K1G	IACT
ALLANTOIN	344S277G0Z	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
Kenaf wet wipe	ALLANTOIN	MEDICELL BIO CO., Ltd.	860f9cc5-a00e-7ccf-e053-2a91aa0a0782	2025-06-24	Warnings	Exact identifier ndc (package): 72944-0001-1 ndc (product): 72944-0001 ndc11 (package): 72944000101 spl id: 384bb90a-444d-547a-e063-6394a90a354b spl set id: 860f9cc5-a00e-7ccf-e053-2a91aa0a0782

Reported adverse events (FAERS/openFDA)#

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