Sani Clean

Manufacturer
Hefei Wenqi Industrial & Trade Co., Ltd
Effective date
2020-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:03

Label at a glance#

ProductSani Clean
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Discard after single use. Do not appy internally. Keep container tightly closed.

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For use in minimizing infections

Warnings

WARNINGS SECTION

For external use only.
Flammable, keep away from fire or flame.
Use only in a well-ventifated area; fumes may be toxic.

When using this product
Do not get into eyes

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control center right away

Do not use

OTC - DO NOT USE SECTION

Do not get into eyes

Do not appy internally.

OTC - WHEN USING SECTION

When using this product
Do not get into eyes

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control center right away

OTC - STOP USE SECTION

Stop use and ask a doctor if
Irritation and redness develop
Condition persists for more than 72 hours
Storage: Protect from freezing. Avoid excessive heat.

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

Discard after single use.
Do not appy internally.
Keep container tightly closed.

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

76991-013-01 100P DRUM76991-013-01 100P DRUM76991-013-02 130P BAG76991-013-02 130P BAG

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76991-013-012022-01-28C16284748780-1d6a99b39-7c9d-a426-e053-dadaa90af4c276991-013 Sani Clean
76991-013-022022-01-28C16284748780-1d6a99b39-7c9d-a426-e053-dadaa90af4c276991-013 Sani Clean

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76991-013-01Sani Clean100 in 1 DRUMCLOTH1001
76991-013-02Sani Clean130 in 1 BAGCLOTH1301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76991-013SANI CLEAN CLOTH [HEFEI WENQI INDUSTRIAL & TRADE CO., LTD]1Legacy NDC, 2 package rows20200924_aff66ada-8860-7440-e053-2995a90aed5d.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
76991-01376991-013-01, 76991-013-02

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
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
aff5d8d1-6faa-2022-e053-2a95a90a81efaff66ada-8860-7440-e053-2995a90aed5d2020-09-23WarningsExact identifier
spl id: aff5d8d1-6faa-2022-e053-2a95a90a81ef
spl set id: aff66ada-8860-7440-e053-2995a90aed5d

Reported adverse events (FAERS/openFDA)#

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