SPECTRUM- ethyl alcohol swab

Spectrum by

Drug Labeling and Warnings

Spectrum by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

■ to decrease bacteria on the skin that could cause disease

Warnings

For external use only: hands

Flammable. Keep away from fire and flame.

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

Stop use and ask a doctor if

■ irritation or redness develops

■ condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

■ wet hands thoroughly with product and allow to dry

■ for children under 6, use only under adult supervision

■ not recommended for infants

Other information

■ do not store above 105 °F

■ may discolor some fabrics

■ harmful to wood finishes and plastics

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SPECTRUM 
ethyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	1.82 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-213-32	20 in 1 PACKAGE; Type 0: Not a Combination Product	05/27/2016	01/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/27/2016	01/01/2022

Labeler - Medline Industries, Inc. (025460908)