Spectrum 62% Hand Sanitizer

Manufacturer
Medline Industries, LP
Effective date
2026-02-11
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:43:58

Label at a glance#

ProductSpectrum 62% Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use onlyunder adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use onlyunder adult supervision
  • not recommended for infants

Other information

OTHER SAFETY INFORMATION

  • do not store above 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, carbomer, diisopropylamine, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Manufacturing Information

SPL UNCLASSIFIED SECTION

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with US and foreign components

www.medline.com

1-800-MEDLINE (633-5463)

REF: HH62G1000

V2 RH22VJO

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label V2 RH22VJOLabel V2 RH22VJO

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN9
581660ethanol 0.62 ML/ML Topical GelSCD9
581660ethanol 62 % Topical GelSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-214-13Spectrum 62% Hand Sanitizer59.147 mL in 1 BOTTLEGEL59.1479
53329-214-70Spectrum 62% Hand Sanitizer443.6 mL in 1 BOTTLEGEL443.69
53329-214-84Spectrum 62% Hand Sanitizer1000 mL in 1 BAGGEL10009
53329-214-85Spectrum 62% Hand Sanitizer354 mL in 1 BOTTLEGEL3549

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53329-21453329-214-13, 53329-214-70, 53329-214-84, 53329-214-85

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Spectrum 62% Hand SanitizerETHYL ALCOHOLMedline Industries, LP6971b7de-039d-292f-e053-2a91aa0a26b22026-02-11WarningsExact identifier
ndc (package): 53329-214-13
ndc (package): 53329-214-84
ndc (package): 53329-214-70
ndc (package): 53329-214-85
ndc (product): 53329-214
ndc11 (package): 53329021470
ndc11 (package): 53329021485
ndc11 (package): 53329021413
ndc11 (package): 53329021484
spl id: 4a8e3675-99a2-b6e6-e063-6394a90a7d48
spl set id: 6971b7de-039d-292f-e053-2a91aa0a26b2

Reported adverse events (FAERS/openFDA)#

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