Wet Wipe

Manufacturer
Zhejiang BeiTao Hygienic Products Co., Ltd.
Effective date
2021-12-17
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:48:14

Label at a glance#

ProductWet Wipe
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

. Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptice Handwash

USE

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only
Flammable - Keep away from fire or flame
When using this product, avoid contact with eyes. In case of
eye contact, rinse with water to remove.
Stop use and ask a doctor if irritation and redness develop.

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 away.

Directions

DOSAGE & ADMINISTRATION SECTION

. Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

40PCS NDC 76906-007-01 40pcs40pcs

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN7
1307051ethanol 0.75 ML/ML Medicated PadSCD7
1307051ethanol 75 % Hand Sanitizer WipesSY7
1307051ethyl alcohol 75 % Topical ClothSY7

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76906-007-01Wet Wipe40 in 1 BAGSWAB407
76906-007-01Wet Wipe5 g in 1 POUCHSWAB57

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76906-007WET WIPE (ALCOHOL) SWAB [ZHEJIANG BEITAO HYGIENIC PRODUCTS CO., LTD.]7Legacy NDC, 2 package rows20241224_a4b3680a-eeb5-22af-e053-2a95a90a965b.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76906-00776906-007-01

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
NameUNIIKind
WATER059QF0KO0RIACT
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
d3562d83-7c0f-9cb7-e053-2995a90a8f7fa4b3680a-eeb5-22af-e053-2a95a90a965b2021-12-17WarningsExact identifier
spl id: d3562d83-7c0f-9cb7-e053-2995a90a8f7f
spl set id: a4b3680a-eeb5-22af-e053-2a95a90a965b

Reported adverse events (FAERS/openFDA)#

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