Home NDC 17312-030-14 Heartburn Relief
Product NDC 17312-030
Requested package NDC 17312-030-14
11-digit product format 173120030
Labeler code 17312
Product ID 17312-030_43ce5061-081c-6f4f-e063-6394a90afc59
Type HUMAN OTC DRUG
Nonproprietary name Carbo MORE
Dosage form TABLET, ORALLY DISINTEGRATING
Route ORAL
Labeler TRP Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-04-15
Substance ACTIVATED CHARCOAL; CHELIDONIUM MAJUS; GINGER; IRIS VERSICOLOR ROOT; POTASSIUM DICHROMATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active strength 6; 6; 6; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS]
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 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Heartburn Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACTIVATED CHARCOAL 6 [hp_X]/1 POTASSIUM DICHROMATE 6 [hp_X]/1 CHELIDONIUM MAJUS 6 [hp_X]/1 SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X]/1 GINGER 6 [hp_X]/1 IRIS VERSICOLOR ROOT 6 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 17312-030-14 Heartburn Relief 50 in 1 BOTTLE TABLET, ORALLY DISINTEGRATING 50 3 17312-030-14 Heartburn Relief 1 in 1 PACKAGE TABLET, ORALLY DISINTEGRATING 1 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACTIVATED CHARCOAL ACTIVE INGREDIENT 2P3VWU3H10 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 CHELIDONIUM MAJUS ACTIVE INGREDIENT 7E889U5RNN HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 GINGER ACTIVE INGREDIENT C5529G5JPQ HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 IRIS VERSICOLOR ROOT ACTIVE INGREDIENT X43D4L3DQC HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 POTASSIUM DICHROMATE ACTIVE INGREDIENT T4423S18FM HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE ACTIVE INGREDIENT 70WT22SF4B HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 ACTIVATED CHARCOAL ACTIVE MOIETY 2P3VWU3H10 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 CHELIDONIUM MAJUS ACTIVE MOIETY 7E889U5RNN HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 DICHROMATE ION ACTIVE MOIETY 9LKY4BFN2V HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 GINGER ACTIVE MOIETY C5529G5JPQ HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 IRIS VERSICOLOR ROOT ACTIVE MOIETY X43D4L3DQC HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 COPOVIDONE INACTIVE INGREDIENT D9C330MD8B HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 LACTOSE INACTIVE INGREDIENT J2B2A4N98G HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 MANNITOL INACTIVE INGREDIENT 3OWL53L36A HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17312-030 HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY] 2 Current NDC, Legacy NDC, 2 package rows 20210112_14bd30e5-a981-597a-e054-00144ff8d46c.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 17312-030-14 17312003014 1 BOTTLE in 1 PACKAGE (17312-030-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE 1 bottle 2015-04-15 0000-00-00 No No Current