INSTANT FOAMING HAND SANITIZER- alcohol soap

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

Buy It Now

Active ingredient:
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Available from:
RD Food Service DBA Restaurant Depot
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
- Use hand sanitizer to reduce microorganisms on the skin. - Use this product when soap and water are not available. Antiseptic
Authorization status:
OTC monograph not final
Authorization number:
56131-701-29

INSTANT FOAMING HAND SANITIZER- alcohol soap

RD Food Service DBA Restaurant Depot

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.

----------

Instant Foaming Hand Sanitizer

Active Ingredient

Ethyl Alcohol 62%

Us es

Use hand sanitizer to reduce microorganisms on the skin.

Use this product when soap and water are not available.

Warnings

For external use only. Do not ingest.

FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.

Avoid contact with eyes. In case of eye contact, flush with large quantities of water, seek medical

attention if irritation persists.

If skin irritation develops, discontinue use. If irritation persists for more than 72 hours, seek medical

attention.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Read the entire label before using this product.

Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands

until dry.

Inactive Ingredients

Water, Propylene Glycol, Acrylic Polymer, Alkyl Phosphate Salts, Fragrance, DC Green #5.

Purpos e

Antiseptic

Alcohol Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Alcohol Foaming Hand Sanitizer

RD_755

INSTANT FOAMING HAND SANITIZER

alcohol soap

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:56 131-70 1

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

0 .6 2 mL in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

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

C2 0 -2 2 ALKYL PHO SPHATE (UNII: L4VKP0 Y7RP)

D&C GREEN NO . 5 (UNII: 8 J6 RDU8 L9 X)

PEG-10 DIMETHICO NE ( 6 0 0 CST) (UNII: 8 PR7V1SVM0 )

RD Food Service DBA Restaurant Depot

Product Characteristics

Color

blue

S core

S hap e

S iz e

Flavor

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:56 131-70 1-29

10 0 0 mL in 1 BAG; Type 0 : No t a Co mbinatio n Pro duct

0 6 /0 1/20 16

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 6 /0 1/20 16

Labeler -

RD Food Service DBA Restaurant Depot (878186774)

Registrant -

Betco Corporation, Ltd. (024492831)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Betco Co rpo ratio n, Ltd.

0 2449 28 31

manufacture(56 131-70 1) , label(56 131-70 1)

Revised: 4/2019

Similar products

Search alerts related to this product

View documents history

Share this information