NDC 54532-0024

Hevert Trauma Roll-On

Arnica Montana Root, Bellis Perennis, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/stem Bark, Hypericum Perforatum, Achillea Millefolium Flowering Top, Ruta Graveolens Flowering Top, And Comfrey Root

Hevert Trauma Roll-On is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Hevert Pharmaceuticals Llc. The primary component is Arnica Montana Root; Bellis Perennis; Calendula Officinalis Flowering Top; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Achillea Millefolium Flowering Top; Ruta Graveolens Flowering Top; Comfrey Root.

Product ID54532-0024_26483b5c-7faf-4c22-90d7-87303fbad8fd
NDC54532-0024
Product TypeHuman Otc Drug
Proprietary NameHevert Trauma Roll-On
Generic NameArnica Montana Root, Bellis Perennis, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/stem Bark, Hypericum Perforatum, Achillea Millefolium Flowering Top, Ruta Graveolens Flowering Top, And Comfrey Root
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2016-04-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHevert Pharmaceuticals LLC
Substance NameARNICA MONTANA ROOT; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWERING TOP; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; ACHILLEA MILLEFOLIUM FLOWERING TOP; RUTA GRAVEOLENS FLOWERING TOP; COMFREY ROOT
Active Ingredient Strength3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 54532-0024-5

1 BOTTLE, WITH APPLICATOR in 1 CARTON (54532-0024-5) > 50 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Start Date2016-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54532-0024-6 [54532002406]

Hevert Trauma Roll-On GEL
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-01

NDC 54532-0024-5 [54532002405]

Hevert Trauma Roll-On GEL
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-04-01

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA ROOT3 [hp_X]/mL

OpenFDA Data

SPL SET ID:dce69e3b-e080-459c-a444-4f84322a7f89
Manufacturer
UNII

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