Spectrum

Manufacturer: Medline Industries, LP
Effective date: 2021-11-17
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 22:26:49

Label at a glance#

ProductSpectrum

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

■ to decrease bacteria on the skin that could cause disease

Dosage and administration

■ wet hands thoroughly with product and allow to dry ■ for children under 6, use only under adult supervision ■ not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only: hands

SPL UNCLASSIFIED SECTION

Flammable. Keep away from fire and flame.

OTC - WHEN USING SECTION

When using this product

■ keep out of eyes. In case of contact with eyes, flush thoroughly with water.

■ avoid contact with broken skin

■ do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if

■ irritation or redness develops

■ condition persists for more than 72 hours

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

■ wet hands thoroughly with product and allow to dry

■ for children under 6, use only under adult supervision

■ not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

■ do not store above 105 °F

■ may discolor some fabrics

■ harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, propylene glycol, glycerin, carbomer, triethanolamine, diazolidinyl urea, aloe barbadensis leaf juice, tocopheryl acetate, methyl paraben, propyl paraben

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Spectrum
ethyl alcohol
WATER
ALCOHOL
CARBOXYPOLYMETHYLENE
PROPYLENE GLYCOL
GLYCERIN
TROLAMINE
DIAZOLIDINYL UREA
ALOE VERA LEAF
ALPHA-TOCOPHEROL ACETATE
METHYLPARABEN
PROPYLPARABEN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53329-213	53329-213-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOXYPOLYMETHYLENE	0A5MM307FC	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
DIAZOLIDINYL UREA	H5RIZ3MPW4	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALPHA-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
PROPYLPARABEN	Z8IX2SC1OH	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d103a03b-349c-e7a7-e053-2a95a90a5e96			3bddd64b-fd13-1628-e054-00144ff8d46c	2021-11-17	Warnings	Exact identifier spl id: d103a03b-349c-e7a7-e053-2a95a90a5e96 spl set id: 3bddd64b-fd13-1628-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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