Home NDC 81183-102 THE FLOWER REMEDY Get Up and Go
Product NDC 81183-102
11-digit product format 811830102
Labeler code 81183
Product ID 81183-102_f8fa5592-f48c-4d9d-b10e-fabb873d400d
Type HUMAN OTC DRUG
Nonproprietary name Gentianella amarella, Ulex europaeus, Larix decidua, Quercus robur, Olea europaea, Castanea sativa, Bromus ramosus, Carbo Vegetabilis
Dosage form LIQUID
Route ORAL
Labeler The Flower Remedy
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-04-26
Substance ACTIVATED CHARCOAL; BROMUS RAMOSUS FLOWER; CASTANEA SATIVA FLOWER; GENTIANELLA AMARELLA FLOWER; LARIX DECIDUA FLOWERING TOP; OLEA EUROPAEA FLOWER; QUERCUS ROBUR FLOWER; ULEX EUROPAEUS FLOWER
Active strength 200; 5; 5; 5; 5; 5; 5; 5 [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 22 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 81183-102-30 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 81183-102-30 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 81183-102-30 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 81183-102-30 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 81183-102-30 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 81183-102-30 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 81183-102-30 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 81183-102-30 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81183-102-30 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 81183-102-30 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 81183-102-30 I Inactivated by FDA 367a005e9d99…383a685ebd0f…
Additional Listing Data#
Finished product Yes
Brand name base THE FLOWER REMEDY Get Up and Go
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GENTIANELLA AMARELLA FLOWER 200 [hp_C]/30mL ULEX EUROPAEUS FLOWER 5 [hp_X]/30mL LARIX DECIDUA FLOWERING TOP 5 [hp_X]/30mL QUERCUS ROBUR FLOWER 5 [hp_X]/30mL OLEA EUROPAEA FLOWER 5 [hp_X]/30mL CASTANEA SATIVA FLOWER 5 [hp_X]/30mL BROMUS RAMOSUS FLOWER 5 [hp_X]/30mL ACTIVATED CHARCOAL 5 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 81183-102-30 THE FLOWER REMEDY Get Up and Go 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81183-102 THE FLOWER REMEDY GET UP AND GO (GENTIANELLA AMARELLA, ULEX EUROPAEUS, LARIX DECIDUA, QUERCUS ROBUR, OLEA EUROPAEA, CASTANEA SATIVA, BROMUS RAMOSUS, CARBO VEGETABILIS) LIQUID [THE FLOWER REMEDY] 1 Current NDC, Legacy NDC, 1 package rows 20210609_52171aaa-8154-46c4-a807-7a7d209aa6cc.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 THE FLOWER REMEDY Get Up and Go GENTIANELLA AMARELLA, ULEX EUROPAEUS, LARIX DECIDUA, QUERCUS ROBUR, OLEA EUROPAEA, CASTANEA SATIVA, BROMUS RAMOSUS, CARBO VEGETABILIS The Flower Remedy 52171aaa-8154-46c4-a807-7a7d209aa6cc 2025-12-03 Warnings Exact identifier ndc (product): 81183-102
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81183-102-30 81183010230 30 mL in 1 BOTTLE, DROPPER (81183-102-30) 30 ml 2021-04-26 0000-00-00 No No Current