Veive CBD Muscle Relaxer

Product NDC

58368-012

11-digit product format

583680012

Labeler code

58368

Product ID

58368-012_d086d571-760b-668d-e053-2995a90a6921

Type

HUMAN OTC DRUG

Nonproprietary name

Arnica Montana, Causticum, Rhamnus Californica, Ruta Graveolens, Taraxacum Officinale, Belladonna, Cimicifuga Racemosa, Gnaphalium Polycephalum, Hypericum Perforatum, Jatropha Curcas, Veratrum Album, Cina, Ignatia Amara, Kali Bromatum, Kali Carbonicum, Lycopodium Clavatum, Scutellaria Lateriflora, Valeriana Officinalis

Dosage form

CREAM

Route

TOPICAL

Labeler

BioLyte Laboratories, LLC

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-11-16

Marketing end

0000-00-00

Substance

ARNICA MONTANA; STRYCHNOS IGNATII SEED; RUTA GRAVEOLENS FLOWERING TOP; SCUTELLARIA LATERIFLORA WHOLE; TARAXACUM OFFICINALE; VALERIAN; VERATRUM ALBUM ROOT; ATROPA BELLADONNA; CAUSTICUM; ARTEMISIA CINA FLOWER; POTASSIUM BROMIDE; POTASSIUM CARBONATE; FRANGULA CALIFORNICA BARK; HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; BLACK COHOSH; PSEUDOGNAPHALIUM OBTUSIFOLIUM; JATROPHA CURCAS SEED

Active strength

4 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g

NDC exclude flag

No

Listing certified through

2022-12-31

Current FDA listing

Historical FDA.report record