SUPPRESS SANITIZIZING WIPES

Manufacturer
Kunming Ansheng Industry & Trade Co., Ltd. | HD Group LLC
Effective date
2020-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:33

Label at a glance#

ProductSUPPRESS SANITIZIZING WIPES
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Rhoroughly wipe hands, fingers and wrists. Be sure to use the entire wipe. Rub hands together until dry. For dirty hands, use first wipe to clean hands, then discard wipe. Sanitize with a second wipe. Discard after single use. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl acohol 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.
  • Recommended for repeated use.

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 keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

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

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

  • Rhoroughly wipe hands, fingers and wrists. Be sure to use the entire wipe.
  • Rub hands together until dry.
  • For dirty hands, use first wipe to clean hands, then discard wipe. Sanitize with a second wipe.
  • Discard after single use.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Pure water USP.

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • Store between 15-30℃ (59-86℉)
  • Avoid freezing and excessive heat about 40℃ (104℉)
  • Dispose of wipe in the proper container after use.
  • Do not flush down the toilet.
  • Lot No. and Expiration date can be found on canister.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

150 wipes in 1 canister.

NDC: 78183-011-01;

150150

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
78183-011-012022-01-28C16284748780-1d6a99b39-60fa-a426-e053-dadaa90af4c2SUPPRESS SANITIZIZING WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78183-011-01SUPPRESS SANITIZIZING WIPES150 U in 1 CANISTERCLOTH1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78183-011SUPPRESS SANITIZIZING WIPES (75% ALCOHOL WIPES) CLOTH [KUNMING ANSHENG INDUSTRY & TRADE CO., LTD.]1Legacy NDC, 1 package rows20200917_af6cc8a4-d2e3-2618-e053-2995a90a61d6.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
78183-01178183-011-01

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
af6c7d0e-3125-12cf-e053-2a95a90a1d9eaf6cc8a4-d2e3-2618-e053-2995a90a61d62020-09-16WarningsExact identifier
spl id: af6c7d0e-3125-12cf-e053-2a95a90a1d9e
spl set id: af6cc8a4-d2e3-2618-e053-2995a90a61d6

Reported adverse events (FAERS/openFDA)#

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