FDA.reportPublic FDA data

BTB Wind

Manufacturer
SCA NuTec
Effective date
2010-04-19
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:39:19

Label at a glance#

ProductBTB Wind
Active ingredientHARPAGOPHYTUM PROCUMBENS ROOT, GLYCYRRHIZA GLABRA, PEPPERMINT, EUCALYPTUS GLOBULUS LEAF
Label structure6 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Harpagophytum procumbens, glycyrrhiza glabra, mentha piperita & eucalyptus leaf

Active Ingredients:

SPL UNCLASSIFIED SECTION

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:

INACTIVE INGREDIENT SECTION

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

WARNINGS SECTION

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]

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of containerimage of container

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCYRRHIZA GLABRA Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
PEPPERMINT Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52338-627-20BTB Wind20000 mL in 1 BOTTLEEXTRACT200001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52338-627BTB WIND (DEVILS CLAW CUT ROOT, LICORICE ROOT, PEPPERMIJNT LEAF, AND EUCALYPTUS LEAF) EXTRACT [SCA NUTEC]11 package rows20100419_0e6c88e4-6e7d-4982-b6d8-d8860bb4e54b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EUCALYPTUS GLOBULUS LEAFACTIVE INGREDIENTS546YLW6E61
GLYCYRRHIZA GLABRAACTIVE INGREDIENT2788Z9758H1
HARPAGOPHYTUM PROCUMBENS ROOTACTIVE INGREDIENT1OYM338E891
PEPPERMINTACTIVE INGREDIENTV95R5KMY2B1
EUCALYPTUS GLOBULUS LEAFACTIVE MOIETYS546YLW6E61
GLYCYRRHIZA GLABRAACTIVE MOIETY2788Z9758H1
HARPAGOPHYTUM PROCUMBENS ROOTACTIVE MOIETY1OYM338E891
PEPPERMINTACTIVE MOIETYV95R5KMY2B1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52338-62752338-627-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
HARPAGOPHYTUM PROCUMBENS ROOT1OYM338E89ACTIB
GLYCYRRHIZA GLABRA2788Z9758HACTIB
PEPPERMINTV95R5KMY2BACTIB
EUCALYPTUS GLOBULUS LEAFS546YLW6E6ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HARPAGOPHYTUMHARPAGOPHYTUM PROCUMBENS ROOTBoironb9819b1b-c541-970d-e053-2995a90a64ed2023-12-21Name fallback
generic name: HARPAGOPHYTUM PROCUMBENS ROOT
HARPAGOPHYTUMHARPAGOPHYTUM PROCUMBENS ROOTBoironc1362af5-3b18-31a7-e053-2995a90a1e8d2023-11-13Name fallback
generic name: HARPAGOPHYTUM PROCUMBENS ROOT
HARPAGOPHYTUMHARPAGOPHYTUM PROCUMBENS ROOTBoironc135154f-e252-dea9-e053-2995a90ac8362023-11-13Name fallback
generic name: HARPAGOPHYTUM PROCUMBENS ROOT

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.