Alcohol wipes

Manufacturer: Wenzhou Bofeng Packaging Co., Ltd.
Effective date: 2020-07-16
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:21:41

Label at a glance#

ProductAlcohol wipes

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Open lid, gently pull back resealable label, remove and use wipe as required. Reseal back after use to avoid evaporation of alcohol.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin.
Apply topically to the skin to help prevent cross contamination.
Recommended for repeated use.
Dries in seconds.

Warnings

WARNINGS SECTION

If swallowed, get medical help or contact a poison control center immediately

OTC - DO NOT USE SECTION

Do not use in eyes. In case of contact, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask doctor if rash/redness or irritation appears/develops and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a poison control center

Directions

DOSAGE & ADMINISTRATION SECTION

Open lid, gently pull back resealable label, remove and use wipe as required.
Reseal back after use to avoid evaporation of alcohol.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79014-002-02 10PCS

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1307051	ethanol 75 % Medicated Pad	PSN	2
1307051	ethanol 0.75 ML/ML Medicated Pad	SCD	2
1307051	ethanol 75 % Hand Sanitizer Wipes	SY	2
1307051	ethyl alcohol 75 % Topical Cloth	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79014-002-01	2022-01-28	C162847	48780-1	d6a99b39-776c-a426-e053-dadaa90af4c2	75% Alcohol water wipes
79014-002-02	2022-01-28	C162847	48780-1	d6a99b39-776c-a426-e053-dadaa90af4c2	75% Alcohol water wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79014-002-01	Alcohol wipes	3.5 g in 1 PATCH	CLOTH	3.5	2
79014-002-01	Alcohol wipes	50 in 1 BAG	CLOTH	50	2
79014-002-02	Alcohol wipes	10 in 1 BAG	CLOTH	10	2
79014-002-02	Alcohol wipes	3.5 g in 1 PATCH	CLOTH	3.5	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79014-002	ALCOHOL WIPES (ALCOHOL) CLOTH [WENZHOU BOFENG PACKAGING CO., LTD.]	2	Legacy NDC, 4 package rows	20200717_aa8a454f-101a-f756-e053-2995a90ae4cf.zip

Products#

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

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

Alcohol wipes
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79014-002	79014-002-01, 79014-002-02

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
aa8aad13-c74e-f3e2-e053-2a95a90ab0ac			aa8a454f-101a-f756-e053-2995a90ae4cf	2020-07-16	Warnings	Exact identifier spl id: aa8aad13-c74e-f3e2-e053-2a95a90ab0ac spl set id: aa8a454f-101a-f756-e053-2995a90ae4cf

Reported adverse events (FAERS/openFDA)#

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