BTB WIND- devils claw cut root, licorice root, peppermijnt leaf, and eucalyptus leaf extract

BTB Wind by

Drug Labeling and Warnings

BTB Wind by is a Animal medication manufactured, distributed, or labeled by SCA NuTec. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Harpagophytum procumbens, glycyrrhiza glabra, mentha piperita & eucalyptus leaf

Active Ingredients:

Devils Claw Cut Root [Harpagophytum procumbens] 10mg per ml
Licorice Root [Glycyrrhiza glabra] 10mg per ml
Peppermijnt Leaf [Mentha piperita] 10mg per ml
Eucalyptus Leaf [Eucalyptus globulus] 10mg per ml

Inactive Ingredients:

Acetic acid glacial and Propionic acid [organic preservatives[Salt,Water

WARNINGS

FOR USE ON ANIMALS ONLY

SPL UNCLASSIFIED SECTION

BTB Wind contains NO animal parts or residues

Imported to the USA by :
Emerald Valley Natural Health Inc, Exeter, NH 03833

Batch No: 94413
Use by Date: 03/12/11

BTB Wind is manufactured in the UK by
SCA Nutec [Provimi Ltd]
Nutec Mill, Eastern Avenue
Lichfield, Staffordshire, WS13 7SE, UK

Exported by :
Equiglobal Ltd
Manningtree, Essex, CO11 1UT, UK

20 Litres/5.283 gallons [US]

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BTB WIND 
devils claw cut root, licorice root, peppermijnt leaf, and eucalyptus leaf extract

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 52338-627
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89) (HARPAGOPHYTUM PROCUMBENS ROOT - UNII:1OYM338E89)	HARPAGOPHYTUM PROCUMBENS ROOT	10 mg  in 1 mL
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (GLYCYRRHIZA GLABRA - UNII:2788Z9758H)	GLYCYRRHIZA GLABRA	10 mg  in 1 mL
PEPPERMINT (UNII: V95R5KMY2B) (PEPPERMINT - UNII:V95R5KMY2B)	PEPPERMINT	10 mg  in 1 mL
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)	EUCALYPTUS GLOBULUS LEAF	10 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52338-627-20	20000 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2010

Labeler - SCA NuTec (233072193)

Establishment
Name	Address	ID/FEI	Business Operations
SCA NuTec		233072193	manufacture