Home NDC 68703-373 NativeRemedies Backache Ease
Product NDC 68703-373
11-digit product format 687030373
Labeler code 68703
Product ID 68703-373_2ab0efa0-68e4-1b30-e063-6294a90ae73e
Type HUMAN OTC DRUG
Nonproprietary name Arnica, Bryonia, Cimicifuga, Hypericum, Ignatia, Kali carb, Nux vom, Rhus tox, Ruta
Dosage form TABLET
Route ORAL
Labeler Silver Star Brands
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-09-07
Substance ACTAEA CIMICIFUGA ROOT; ARNICA ANGUSTIFOLIA FLOWER; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM; POTASSIUM CARBONATE; RUTA GRAVEOLENS FLOWERING TOP; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON RADICANS LEAF
Active strength 12; 12; 12; 12; 12; 12; 12; 12; 12 [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801; [hp_C]/1801
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base NativeRemedies Backache Ease
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RUTA GRAVEOLENS FLOWERING TOP 12 [hp_C]/1801 HYPERICUM PERFORATUM 12 [hp_C]/1801 STRYCHNOS NUX-VOMICA SEED 12 [hp_C]/1801 ARNICA ANGUSTIFOLIA FLOWER 12 [hp_C]/1801 BRYONIA ALBA ROOT 12 [hp_C]/1801 POTASSIUM CARBONATE 12 [hp_C]/1801 STRYCHNOS IGNATII SEED 12 [hp_C]/1801 ACTAEA CIMICIFUGA ROOT 12 [hp_C]/1801 TOXICODENDRON RADICANS LEAF 12 [hp_C]/1801
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68703-373-80 NativeRemedies Backache Ease 180 in 1 BOTTLE, GLASS TABLET 180 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68703-373 NATIVEREMEDIES BACKACHE EASE (ARNICA, BRYONIA, CIMICIFUGA, HYPERICUM, IGNATIA, KALI CARB, NUX VOM, RHUS TOX, RUTA) TABLET [SILVER STAR BRANDS] 4 Current NDC, Legacy NDC, 1 package rows 20250103_c6259789-438a-211a-e053-2995a90aa5c4.zip
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 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join NativeRemedies Backache Ease ARNICA, BRYONIA, CIMICIFUGA, HYPERICUM, IGNATIA, KALI CARB, NUX VOM, RHUS TOX, RUTA Silver Star Brands c6259789-438a-211a-e053-2995a90aa5c4 2025-01-01 Warnings Exact identifier ndc (product): 68703-373
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68703-373-80 68703037380 180 TABLET in 1 BOTTLE, GLASS (68703-373-80) 180 tablet 2021-09-07 0000-00-00 No No Current