SYNOFOAM- teat dip liquid

Synofoam by

Drug Labeling and Warnings

Synofoam by is a Animal medication manufactured, distributed, or labeled by Quat-Chem Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Synofoam

Shake well before use.
Store in ambient temperatures.
FOR PROFESSIONAL COMMERCIAL USE ONLY.
NOT FOR HUMAN USE.
KEEP OUT OF THE REACH OF CHILDREN.

Quat-Chem Ltd.
1-4 Sandfield Industrial Park,
Dodgson Street,
Rochdale, Greater Manchester
United Kingdom
OL16 5SJ
www.quatchem.com
sales@quatchem.co.uk
Tel: +44(0)1706 344 797

EN ISO 9001:2008 QMS
GMP ISO 22716:2007

Manufactured in the UK

DESCRIPTION
▪ Extremely effective, broad-spectrum disinfectant
▪ Formulation contains a 12% specially balanced emollient blend
▪ Includes Aloe Vera, Pure Peppermint Oil & Lanolin
▪ Reduces dehydration of the epidermis, enhancing the condition of the teat
▪ Formulation does not require dilution in preparation for dipping or spraying the teat
▪ Effective foam cleaning action

DIRECTIONS FOR USE
Pre-Milking: Wash or spray teats and base of udder with product. Apply using a foaming cup. Allow 15 seconds contact time. Dry thoroughly with paper towel or udder cloth.

ANTIMICROBIAL EFFICACY
Synofoam passes EN 1656:2000 (phase 2/step 1) Quantitative Test for the evaluation of Bactericidal Activity of Chemical Disinfectants and Antiseptics used in the Veterinary and Agricultural Fields, giving > 99.999% kill for the following environmental organisms frequently implicated in common teat infections.
- Streptococcus dysgalactiae
- Streptococcus uberis
- Streptococcus agalactiae
- Staphylococcus epidermidis
- Staphylococcus aureus
- Escherichia coli
- Enterococcus hirae
Active Ingredients: 1.2% Lactic Acid, 0.9% Phenoxyethanol and 0.8% Phmb
See Packaging For:
Manu Manufactured Date
Expiration Date
Batch Numbe

NDC Number:

Synofoam representative label

INGREDIENTS AND APPEARANCE

SYNOFOAM 
teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 69260-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.7 g  in 1 L
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.5   in 1 L

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69260-002-05	5 L in 1 DRUM
2	NDC: 69260-002-25	25 L in 1 DRUM
3	NDC: 69260-002-20	200 L in 1 DRUM
4	NDC: 69260-002-10	1000 L in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/16/2016

Labeler - Quat-Chem Ltd. (458052420)

Establishment
Name	Address	ID/FEI	Business Operations
Quat-Chem Ltd.		458052420	manufacture, api manufacture, label, pack