FDA.reportPublic FDA data

SUPPRESS Hand Sanitizing Wipes

Manufacturer
HD Group LLC
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:59

Label at a glance#

ProductSUPPRESS Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Thoroughly 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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) 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.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help decrease 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

  • Thoroughly 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.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)
  • 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water USP

Distributed By

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Distributed by:

HD Group LLC

335 N Edgewood Ln, Suite 130

Eagle, ID 83616

SUPPRESS Hand Sanitizing Wipes- 150 Wipes Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

150 Wipes

NDC: 77343-101-01

SUPPRESS Hand Sanitizing Wipes- 150SUPPRESS Hand Sanitizing Wipes- 150

SUPPRESS Hand Sanitizing Wipes- 75 Wipes Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75 Wipes

NDC: 77343-101-02

SUPPRESS Hand Sanitizing Wipes- 75 LabelSUPPRESS Hand Sanitizing Wipes- 75 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN2
1307051ethanol 0.75 ML/ML Medicated PadSCD2
1307051ethanol 75 % Hand Sanitizer WipesSY2
1307051ethyl alcohol 75 % Topical ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77343-101-012024-01-30C16284748780-11030e365-4efa-111a-e063-dadaa90a10e2SUPPRESS Hand Sanitizing Wipes
77343-101-022024-01-30C16284748780-11030e365-4efa-111a-e063-dadaa90a10e2SUPPRESS Hand Sanitizing Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77343-101-01SUPPRESS Hand Sanitizing Wipes612 mL in 1 CANISTERCLOTH6122
77343-101-02SUPPRESS Hand Sanitizing Wipes364 mL in 1 CANISTERCLOTH3642

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77343-101SUPPRESS HAND SANITIZING WIPES (ALCOHOL) CLOTH [HD GROUP LLC]2Legacy NDC, 2 package rows20220115_aae519cc-4e69-2604-e053-2a95a90aac87.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
77343-10177343-101-01, 77343-101-02

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
d590ee08-230f-240f-e053-2995a90a83afaae519cc-4e69-2604-e053-2a95a90aac872022-01-14WarningsExact identifier
spl id: d590ee08-230f-240f-e053-2995a90a83af
spl set id: aae519cc-4e69-2604-e053-2a95a90aac87

Reported adverse events (FAERS/openFDA)#

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