JUSTICE COTTON CANDY SCENTED ANTI-BACTERIAL HAND SANITIZER - CAT- alcohol gel

United States - English - NLM (National Library of Medicine)

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Active ingredient:
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Available from:
Tween Brands, Inc.
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
- For hand washing to decrease bacteria on the skin. - Recommended for repeated use.
Authorization status:
OTC monograph not final
Authorization number:
60637-229-30

JUSTICE COTTON CANDY SCENTED ANTI-BACTERIAL HAND SANITIZER - CAT-

alcohol gel

Tween Brands, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Justice Cotton Candy Scented Anti-bacterial Hand Sanitizer – Cat

Drug Facts

Active ingredient

Alcohol 62%

Purpos e

Antiseptic

Us e

For hand washing to decrease bacteria on the skin.

Recommended for repeated use.

Warnings

Flammable, keep away from fire or flame.

For external use only.

Do not use

in the eyes or apply over large areas of the body.

In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Use only as directed.

Do not drink. If taken internally, it will produce serious gastric disturbances

Stop use and ask a doctor if

Irritation 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 without wiping.

Supervise children in the use of this product.

Other information

Store below 105°F (40.5° C).

May discolor some fabrics.

Expiry Date:06/2023

Inactive ingredients

Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl Propanol, Polyethylene

Terephthalate, Acrylates Copolymer, Red 40.

Package Labeling:

JUSTICE COTTON CANDY SCENTED ANTI-BACTERIAL HAND SANITIZER -

CAT

alcohol gel

Tween Brands, Inc.

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 0 6 37-229

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)

ALCOHOL

6 20 mg in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

GLYCERIN (UNII: PDC6 A3C0 OX)

PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)

CARBO XYPO LYMETHYLENE (UNII: 0 A5MM30 7FC)

AMINO METHYLPRO PANO L (UNII: LU49 E6 6 26 Q)

BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID CO PO LYMER ( 18 0 0 0 MW) (UNII:

JZ1374NL9 E)

FD&C RED NO . 4 0 (UNII: WZB9 127XOA)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:6 0 6 37-229 -

30 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 9 /21/20 19

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt333E

0 9 /21/20 19

Labeler -

T ween Brands, Inc. (965758188)

Revised: 11/2019

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