FDA.reportPublic FDA data

Define Health Alcohol Wipes

Manufacturer
Define Health, LLC
Effective date
2021-12-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:23:23

Label at a glance#

ProductDefine Health Alcohol Wipes
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 75%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • to decrease bacteria on the skin
  • recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

Flammable, keep product away from fire or flame

OTC - WHEN USING SECTION

When using this product keep away from eyes.In case of contact,rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • rub wipe thoroughly over all surfaces of both hands and allow to dry
  • supervise children under 6 years old
  • not recommended for infants
  • discard wipe in trash;do not flush

INACTIVE INGREDIENT SECTION

Inactive ingredients Benzalkonium Chloride, water

SPL UNCLASSIFIED SECTION

50 WIPES

1 Wipe = 140mm x 200mm

5.5in x 7.9in

MANUFACTURED FOR DEFINE HEALTH, LLC

6065 Roswell Road Ste 940

Atlanta GA 30328

MANUFACTURED BY HENAN MEISHIYU SANITARY PRODUCTS CO., LTD

MADE IN CHINA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DEFINE HEALTH

ALCOHOL WIPES

ANTISEPTIC HAND SANITIZER

CONTAINS 75% ALCOHOL

50 WIPES

20200903 define health wipes layout China (1)20200903 define health wipes layout China (1)

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80444-00180444-001-50

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
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d30aa7bb-9d3a-361c-e053-2a95a90afc8cb0153aa3-7739-df63-e053-2995a90a4ec62021-12-13WarningsExact identifier
spl id: d30aa7bb-9d3a-361c-e053-2a95a90afc8c
spl set id: b0153aa3-7739-df63-e053-2995a90a4ec6

Reported adverse events (FAERS/openFDA)#

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