SafetyMax Alcohol wipes

Manufacturer: Kunming Ansheng Industry & Trade Co., Ltd.
Effective date: 2020-09-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:49

Label at a glance#

ProductSafetyMax Alcohol wipes

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

Open flip top when in use, pull out one wipe at a time for use. Close after use to prevent wipes from drying out.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75.0% v/v.

Purpose

OTC - PURPOSE SECTION

To reduce bacteria on the skin and help prevent cross contamination.

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age.
on open skin wounds

OTC - WHEN USING SECTION

When using this product do not use in or contact the eyes or damaged skin. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts. These may be signs of a serious condition.

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

Open flip top when in use, pull out one wipe at a time for use.
Close after use to prevent wipes from drying out.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Pure water.

OTHER INFORMATION

OTHER SAFETY INFORMATION

• Store in a well-ventilated place.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 wipes in 1 canister.

NDC: 78183-010-01;

100p

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1307051	ethanol 75 % Medicated Pad	PSN	1
1307051	ethanol 0.75 ML/ML Medicated Pad	SCD	1
1307051	ethanol 75 % Hand Sanitizer Wipes	SY	1
1307051	ethyl alcohol 75 % Topical Cloth	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78183-010-01	2022-01-28	C162847	48780-1	d6a99b39-9514-a426-e053-dadaa90af4c2	SafetyMax 75% ALCOHOL WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78183-010-01	SafetyMax Alcohol wipes	100 U in 1 CANISTER	CLOTH	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78183-010	SAFETYMAX ALCOHOL WIPES (75% ALCOHOL WIPES) CLOTH [KUNMING ANSHENG INDUSTRY & TRADE CO., LTD.]	1	Legacy NDC, 1 package rows	20200904_ae733f22-6a28-853c-e053-2a95a90ae9a9.zip

Products#

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

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

SafetyMax Alcohol wipes
75% Alcohol Wipes
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78183-010	78183-010-01

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
ae72b6f4-8d8a-6b22-e053-2a95a90a8982			ae733f22-6a28-853c-e053-2a95a90ae9a9	2020-09-03	Warnings	Exact identifier spl id: ae72b6f4-8d8a-6b22-e053-2a95a90a8982 spl set id: ae733f22-6a28-853c-e053-2a95a90ae9a9

Reported adverse events (FAERS/openFDA)#

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