NDC 54532-0010

Hevert Stress Relief

Black Cohosh, Anamirta Cocculus Seed, Cypripedium Parvifolum Root, Strychnos Ignatii Seed, Lilium Lancifolium Flowering Top, Passiflora Incarnata Flowering Top, Platinum, Valerian, And Zinc Valerate Dihydrate

Hevert Stress Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Hevert Arzneimittel Gmbh & Co. Kg. The primary component is Anamirta Cocculus Seed; Black Cohosh; Cypripedium Parviflorum Var. Pubescens Root; Lilium Lancifolium Flowering Top; Passiflora Incarnata Flowering Top; Platinum; Strychnos Ignatii Seed; Valerian; Zinc Valerate Dihydrate.

Product ID54532-0010_72687047-f336-4b57-83d5-676e6407022f
NDC54532-0010
Product TypeHuman Otc Drug
Proprietary NameHevert Stress Relief
Generic NameBlack Cohosh, Anamirta Cocculus Seed, Cypripedium Parvifolum Root, Strychnos Ignatii Seed, Lilium Lancifolium Flowering Top, Passiflora Incarnata Flowering Top, Platinum, Valerian, And Zinc Valerate Dihydrate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2013-02-15
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHevert Arzneimittel GmbH & Co. KG
Substance NameANAMIRTA COCCULUS SEED; BLACK COHOSH; CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT; LILIUM LANCIFOLIUM FLOWERING TOP; PASSIFLORA INCARNATA FLOWERING TOP; PLATINUM; STRYCHNOS IGNATII SEED; VALERIAN; ZINC VALERATE DIHYDRATE
Active Ingredient Strength6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 54532-0010-4

10 BLISTER PACK in 1 CARTON (54532-0010-4) > 10 TABLET in 1 BLISTER PACK
Marketing Start Date2013-02-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54532-0010-4 [54532001004]

Hevert Stress Relief TABLET
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-02-15

NDC 54532-0010-5 [54532001005]

Hevert Stress Relief TABLET
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-02-15

Drug Details

Active Ingredients

IngredientStrength
BLACK COHOSH4 [hp_X]/1

OpenFDA Data

SPL SET ID:7ea167c0-5d81-473d-ba94-b0c97e06a07f
Manufacturer
UNII

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.