INMO 70% Alcohol Hand Gel (30ml)

Manufacturer
NTML Group Ltd
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:44

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Rub dime sized amount between hands until dry Supervise children in the use of this product In the case of eye contact, rinse eyes thoroughly with water

Storage and handling

Store below 105 F May discolour some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Hand Sanitizer with NDC 00000-000 is a a human over the counter drug product labeled by NTML Group Ltd. The generic name of Hand Sanitizer is alcohol. The product's dosage form is gel and is administered via topical form.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flame

Do not drink

If taken internally will produce serious gastric disturbances

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product avoid the eyes and mucous membrane

In the case of eyes or mucous membranes contact, rinse area thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens, redness or irritation develops

If condition persists for more than 3 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub dime sized amount between hands until dry

Supervise children in the use of this product

In the case of eye contact, rinse eyes thoroughly with water

Other information

STORAGE AND HANDLING SECTION

Store below 105 F

May discolour some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aminomethyl Propanol, Carbomer, Glycerin, Propylene Glycol, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70% Alcohol Gel

30 mL (1 fl oz) 30 ml label30 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77366-001-012021-07-23C16284748780-1c7ccaba7-24f3-fd44-e053-dadaa90aa01bINMO 70% Alcohol Hand Gel (30ml)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77366-001-01Hand Sanitizer30 mL in 1 BOTTLEGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77366-001HAND SANITIZER (ALCOHOL) GEL [NTML GROUP LTD]1Legacy NDC, 1 package rows20200506_a46aa499-ae70-2df8-e053-2a95a90a86ad.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77366-00177366-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
a46aa4c7-d01e-3057-e053-2a95a90a7e4aa46aa499-ae70-2df8-e053-2a95a90a86ad2020-04-29WarningsExact identifier
spl id: a46aa4c7-d01e-3057-e053-2a95a90a7e4a
spl set id: a46aa499-ae70-2df8-e053-2a95a90a86ad

Reported adverse events (FAERS/openFDA)#

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