SPECTRUM HAND SANITIZER WIPES- alcohol wipes cloth

SPECTRUM HAND SANITIZER WIPES by

Drug Labeling and Warnings

SPECTRUM HAND SANITIZER WIPES by is a Otc medication manufactured, distributed, or labeled by Medline Industries, Inc.. 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

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

Stop use and ask a doctor if

irritation or redness develops
condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

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

not recommended for infants

other information

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

Inactive ingredients

Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

Uses

to decrease bacteria on the skin that could cause disease

recommended for repeated use

Directions

wet hands thoroughly with product and allow to dry without wiping
not recommended for infants

PRINCIPAL DISPLAY PANEL

20 WIPES, NDC: 53329-998-01

PRINCIPAL DISPLAY PANEL

50 WIPES, NDC: 53329-998-02

PRINCIPAL DISPLAY PANEL

160 WIPES, NDC: 53329-998-03

INGREDIENTS AND APPEARANCE

SPECTRUM HAND SANITIZER WIPES 
alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-998
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPANEDIOL (UNII: 5965N8W85T)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-998-01	20 in 1 PACKAGE	04/30/2021
1		1.32 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53329-998-02	50 in 1 CANISTER	04/30/2021
2		2.55 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53329-998-03	160 in 1 CANISTER	04/30/2021
3		1.2 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/30/2021

Labeler - Medline Industries, Inc. (025460908)