Sani-Ultra Wipes

Manufacturer
Kunming Ansheng Industry & Trade Co., Ltd.
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:58

Label at a glance#

ProductSani-Ultra Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure11 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

Isopropyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antibacterial;

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to reduce bacteria.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame, heat, spark, electrical.

Do not use

OTC - DO NOT USE SECTION

Do not use on or around the eyes or damaged skin.

OTC - WHEN USING SECTION

When using this product do not use in or contact the eyes, ears, and mouth.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Contact medical help or poison control immediatedly, if swallowed.

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 wipes in 1 canister.

NDC: 78183-020-01;

sanisani

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78183-020-012022-01-28C16284748780-1d6a99b39-c748-a426-e053-dadaa90af4c270% Isopropyl Alcohol (Sani-Ultra)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78183-020-01Sani-Ultra Wipes100 U in 1 CANISTERCLOTH1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78183-020SANI-ULTRA WIPES (70% ISOPROPYL ALCOHOL) CLOTH [KUNMING ANSHENG INDUSTRY & TRADE CO., LTD.]1Legacy NDC, 1 package rows20200818_acd4c45f-cb00-8577-e053-2a95a90a88dd.zip

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
78183-02078183-020-01

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
ISOPROPYL ALCOHOLND2M416302ACTIB

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
acd461b5-12ab-8735-e053-2a95a90a8f00acd4c45f-cb00-8577-e053-2a95a90a88dd2020-08-14WarningsExact identifier
spl id: acd461b5-12ab-8735-e053-2a95a90a8f00
spl set id: acd4c45f-cb00-8577-e053-2a95a90a88dd

Reported adverse events (FAERS/openFDA)#

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