Alcohol

Manufacturer
SUHAN AEROSOLS
Effective date
2020-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:17

Label at a glance#

ProductPHARMACYS PRESCRIPTION INSTANT HAND SANITIZER-MOISTURIZERS AND VITAMIN E WITH SECURITY CLIP
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Apply as needed on your palms and thoroughly spread on both hands.  Rub into skin until dry. Other information Store at room 20° C (68° to 77°F) May discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Do not ingest or swallow.
Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed on your palms and thoroughly spread on both hands. Rub into skin until dry.

Other information

  • Store at room 20° C (68° to 77°F)
  • May discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbopol, Triethanolamine, Fragrance, Tocopheryl Acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73398-111-012022-01-28C16284748780-1d6a99b39-e05a-a426-e053-dadaa90af4c283b59fa7-0354-4442-b053-3de0f35624e1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73398-111-01PHARMACYS PRESCRIPTION INSTANT HAND SANITIZER-MOISTURIZERS AND VITAMIN E WITH SECURITY CLIP2 in 1 PACKAGEGEL21
73398-111-01PHARMACYS PRESCRIPTION INSTANT HAND SANITIZER-MOISTURIZERS AND VITAMIN E WITH SECURITY CLIP60 mL in 1 BOTTLE, PLASTICGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73398-111PHARMACYS PRESCRIPTION INSTANT HAND SANITIZER-MOISTURIZERS AND VITAMIN E WITH SECURITY CLIP (ALCOHOL) GEL [SUHAN AEROSOLS]1Legacy NDC, 2 package rows20200821_83b59fa7-0354-4442-b053-3de0f35624e1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73398-11173398-111-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
36be745a-c2ab-41d0-95f9-f718c72e2c0383b59fa7-0354-4442-b053-3de0f35624e12020-08-10WarningsExact identifier
spl id: 36be745a-c2ab-41d0-95f9-f718c72e2c03
spl set id: 83b59fa7-0354-4442-b053-3de0f35624e1

Reported adverse events (FAERS/openFDA)#

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