Home NDC 62795-1044 Reboost
Product NDC 62795-1044
11-digit product format 627951044
Labeler code 62795
Product ID 62795-1044_8b49b20a-1ee8-4625-8c04-280c39ef2197
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR
Dosage form TABLET
Route ORAL
Labeler MediNatura Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-01-05
Substance ACONITUM NAPELLUS; BRYONIA ALBA ROOT; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; IPECAC; LACHESIS MUTA VENOM; PHOSPHORUS; SULFUR; VINCETOXICUM HIRUNDINARIA ROOT; ZINC ACETATE ANHYDROUS; ZINC GLUCONATE
Active strength 3; 3; 20; 6; 5; 3; 10; 8; 4; 6; 2; 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; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Copper Absorption Inhibitor [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Reboost
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 3 [hp_X]/1 BRYONIA ALBA ROOT 3 [hp_X]/1 EUPATORIUM PERFOLIATUM FLOWERING TOP 20 [hp_X]/1 LACHESIS MUTA VENOM 6 [hp_X]/1 GOLDENSEAL 5 [hp_X]/1 PHOSPHORUS 3 [hp_X]/1 VINCETOXICUM HIRUNDINARIA ROOT 10 [hp_X]/1 ZINC GLUCONATE 8 [hp_X]/1 ZINC ACETATE ANHYDROUS 4 [hp_X]/1 CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 6 [hp_X]/1 IPECAC 2 [hp_X]/1 SULFUR 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62795-1044-2 Reboost 1 in 1 CARTON TABLET 1 2 62795-1044-2 Reboost 60 in 1 BOTTLE TABLET 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62795-1044 REBOOST (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR) TABLET [MEDINATURA INC.] 2 Current NDC, Legacy NDC, 2 package rows 20230609_781c1a63-5210-4069-8427-bc7df68d6d63.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 Reboost ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR MediNatura Inc. 781c1a63-5210-4069-8427-bc7df68d6d63 2023-06-05 Warnings Exact identifier ndc (product): 62795-1044
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62795-1044-2 62795104402 1 BOTTLE in 1 CARTON (62795-1044-2) / 60 TABLET in 1 BOTTLE 1 bottle 2022-01-05 0000-00-00 No No Current