myabetic Alcohol Prep Pads

Manufacturer: YIWU HAODING MEDICAL CO.,LTD
Effective date: 2023-03-03
Label type: HUMAN OTC DRUG LABEL
Version: 74
Source: full-release
Hydrated at: 2026-05-31 23:54:22

Label at a glance#

Productmyabetic Alcohol Prep Pads

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

For preparation of the skin prior to an injection.

Dosage and administration

Apply alcohol as needed to clean intended area. Discard after single use. Storage: Keep at room temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

For preparation of the skin prior to an injection.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply alcohol as needed to clean intended area. Discard after single use.

Storage: Keep at room temperature.

WARNINGS SECTION

For external use only.

Flammable, keep away from heat and flame.

Do not use: with electrocautery procedures or in eyes.

Stop use: If redness or irritation develops. If condition continues for more than 72 hours, consult a physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested, do not induce vomiting. Get medical help or contact a Poison Control Center immediately.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	74
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	74
797544	isopropyl alcohol 70 % Medicated Pad	SY	74
797544	isopropyl alcohol 70 % Topical Cloth	SY	74
797544	isopropyl alcohol 70 % Topical Swab	SY	74

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69139-216-01	2025-01-30	C162847	48780-1	f386c649-f709-0266-e053-dadaa90a7c1a	71001cac-e6f7-4b05-88c6-e65abfd69e84
69139-216-01	2023-03-06	C162847	48780-1	f386c649-f709-0266-e053-dadaa90a7c1a	71001cac-e6f7-4b05-88c6-e65abfd69e84
69139-216-01	2023-01-30	C162847	48780-1	f386c649-f709-0266-e053-dadaa90a7c1a	71001cac-e6f7-4b05-88c6-e65abfd69e84

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69139-216-01	myabetic Alcohol Prep Pads	0.3 g in 1 PACKAGE	SWAB	0.3		74
69139-216-01	myabetic Alcohol Prep Pads	1 in 1 PACKAGE	SWAB	1		74

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69139-216	MYABETIC ALCOHOL PREP PADS (ALCOHOL) SWAB [YIWU HAODING MEDICAL CO.,LTD]	74	Legacy NDC, 2 package rows	20230307_71001cac-e6f7-4b05-88c6-e65abfd69e84.zip

Products#

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

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

myabetic Alcohol Prep Pads
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69139-216	69139-216-01

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
f60c7828-29ca-aa0c-e053-2995a90a84af			71001cac-e6f7-4b05-88c6-e65abfd69e84	2023-03-03	Warnings	Exact identifier spl id: f60c7828-29ca-aa0c-e053-2995a90a84af spl set id: 71001cac-e6f7-4b05-88c6-e65abfd69e84

Reported adverse events (FAERS/openFDA)#

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