GERM-X ADVANCED- advanced hand sanitizer gel

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

Buy It Now

Active ingredient:
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Available from:
Vi Jon, Inc
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
Antiseptic - to decrease bacteria on the skin that could cause disease - recommend for repeated use - irritation or redness develops - condition persists for more than 72 hours
Authorization status:
OTC monograph not final
Authorization number:
11344-746-16, 11344-746-26, 11344-746-32, 11344-746-34, 11344-746-38, 11344-746-45, 11344-746-49, 11344-746-86, 11344-746-88

GERM-X ADVANCED- advanced hand sanitizer gel

Vi Jon, 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.

----------

Germ-X 746.000/AA

claims

Introducting the most effective Germ-x formula ever

*Effective at eliminating more than 99.99% of may common harmful germs *& bacteria in as little as 15

seconds

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

to decrease bacteria on the skin that could cause disease

recommend for repeated use

Warnings

For external use only: hands

Flammable. Keep away from heat 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 thoroghly with product and allow to dry without wiping

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, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30

alkyl acrylate crosspolymer, fragrance, benzophenone-4

Ques tions

1-866-MY GERMX - 1-866-694-3769

Adverse reactions

Manufactured By: Vi-Jon, Inc.

8515 Page Ave

St. Louis, MO 63114

www.germx.com

SDS MO-15036

SDA WI-2486

DSP-MO-28

DSP-MO-34

Pat.9,161,982

746.00/746AA

principal display panel

germ-X

ADVANCED

Hand Sanitizer

MORE EFFECTIVE FORMULA

kills more than 99.99% of germs

PATENTED

FORMULA

Original Scent

33.8 FL OZ (1 L)

GERM-X ADVANCED

advanced hand sanitizer gel

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:11344-746

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

70 0 mg in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

wa ter (UNII: 0 59 QF0 KO0 R)

GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10 N)

GLYCERIN (UNII: PDC6 A3C0 OX)

ISO PRO PYL MYRISTATE (UNII: 0 RE8 K4LNJS)

.ALPHA.-TO CO PHERO L ACETATE (UNII: 9 E8 X8 0 D2L0 )

CARBO MER INTERPO LYMER TYPE A ( ALLYL SUCRO SE CRO SSLINKED) (UNII: 59 TL3WG5CO)

SULISO BENZO NE (UNII: 1W6 L6 29 B4K)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:11344-746 -

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

Pro duc t

0 8 /21/20 17

2

NDC:11344-746 -

236 mL in 1 BOTTLE, PUMP; Type 0 : No t a Co mbinatio n Pro duct

0 8 /21/20 17

3

NDC:11344-746 -

9 46 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 8 /21/20 17

4

NDC:11344-746 -

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

Pro duc t

0 8 /21/20 17

5

NDC:11344-746 -

29 5 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 8 /21/20 17

6

NDC:11344-746 -

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

Pro duc t

0 8 /21/20 17

7

NDC:11344-746 -

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

Pro duc t

0 8 /21/20 17

8

NDC:11344-746 -

19 9 9 mL in 1 BOTTLE, PLASTIC; Type 0 : No t a Co mbinatio n

Pro duc t

0 8 /21/20 17

9

NDC:11344-746 -

10 0 0 mL in 1 BOTTLE, PUMP; Type 0 : No t a Co mbinatio n

Pro duc t

0 8 /21/20 17

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 rt333A

0 8 /21/20 17

Labeler -

Vi Jon, Inc (150931459)

Registrant -

Vi-Jon, Inc. (790752542)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Vi-Jo n, Inc.

0 8 8 520 6 6 8

ma nufa c ture (11344-746 )

Vi Jon, Inc

Revised: 5/2020

Similar products

Search alerts related to this product

View documents history

Share this information