Antibacterial PE film

Manufacturer: DH Investment Co Ltd
Effective date: 2020-06-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:19:20

Label at a glance#

ProductAntibacterial PE film

Active ingredientTITANIUM DIOXIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide

INACTIVE INGREDIENT SECTION

polyethylene, copper

OTC - PURPOSE SECTION

Antibacterial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

apply proper amount where needed

WARNINGS SECTION

For external use only

When using this product

■ if following abnormal symptoms persist, discontinue use

Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

■ Stop immediately and consult a doctor if you experience

1) Hypersensitivity symptoms such as erythema, itching and dermatitis.

2) Skin Irritation

3) Following Instructions when using medication

(1) For external use only (Do not use internally)

(2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

■ Do not use the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin.

It is not recommended to use this one areas that have been medically treated with a cast or bandage.

DOSAGE & ADMINISTRATION SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79234-0001-1	2022-01-28	C162847	48780-1	d6a99b39-f646-a426-e053-dadaa90af4c2	a909f7e2-21ac-cf9e-e053-2995a90a6f90

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79234-0001-1	Antibacterial PE film	1 g in 1 PACKAGE	FILM	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79234-0001	ANTIBACTERIAL PE FILM (TITANIUM DIOXIDE) FILM [DH INVESTMENT CO LTD]	2	Legacy NDC, 1 package rows	20200628_a909f7e2-21ac-cf9e-e053-2995a90a6f90.zip

Products#

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

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

Antibacterial PE film
titanium dioxide
COPPER
HIGH DENSITY POLYETHYLENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79234-0001	79234-0001-1

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
COPPER	789U1901C5	IACT
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
HIGH DENSITY POLYETHYLENE	UG00KM4WR7	IACT

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
a90ebc32-7f8c-591f-e053-2995a90a7761			a909f7e2-21ac-cf9e-e053-2995a90a6f90	2020-06-27	Warnings	Exact identifier spl id: a90ebc32-7f8c-591f-e053-2995a90a7761 spl set id: a909f7e2-21ac-cf9e-e053-2995a90a6f90

Reported adverse events (FAERS/openFDA)#

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