FDA.reportPublic FDA data

009 Spectrum Advanced 70% Packet

Manufacturer
Medline Industries, LP
Effective date
2026-08-25
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-08-29 01:01:38

Label at a glance#

ProductSpectrum
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

do not store above 105ºF may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

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 only under adult supervision
  • not recommended for infants

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, diisopropylamine, glycerin, isopropyl myristate, tocopheryl acetate, water

Manufacturing Information

SPL UNCLASSIFIED SECTION

Manufactored 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

REF: HH70GPACKET

V1 RA22VJO

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BackBack

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53329-009-022022-08-16C16284748780-1e4f33bdf-b19c-d8a0-e053-dadaa90a6e4e009 Spectrum Advanced 70% Packet
53329-009-022022-08-16C16284748780-1e4f33bdf-b19c-d8a0-e053-dadaa90a6e4e009 Spectrum Advanced 70% Packet
53329-009-022022-07-29C16284748780-1e4f33bdf-b19c-d8a0-e053-dadaa90a6e4e009 Spectrum Advanced 70% Packet
53329-009-022022-07-29C16284748780-1e4f33bdf-b19c-d8a0-e053-dadaa90a6e4e009 Spectrum Advanced 70% Packet

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53329-00953329-009-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
DIISOPROPYLAMINEBR9JLI40NOIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72026-02-10full-release2026-06-01 01:43:50

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
SpectrumETHYL ALCOHOLMedline Industries, LP428b1cb9-7db8-3141-e054-00144ff8d46c2026-08-25WarningsExact identifier
ndc (package): 53329-009-02
ndc (product): 53329-009
ndc11 (package): 53329000902
spl id: 59e61fc9-7163-63ba-e063-6394a90a5f28
spl set id: 428b1cb9-7db8-3141-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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