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

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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BTB Wind

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

FOR USE ON ANIMALS ONLY

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]

image of container

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

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

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

Labeler - SCA NuTec (233072193)

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