Heartburn Relief

Product NDC
17312-030
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 · 28 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage17312-030-14f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage17312-030-142ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage17312-030-14a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage17312-030-14cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage17312-030-14cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage17312-030-14302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage17312-030-14ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage17312-030-140efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage17312-030-14ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage17312-030-14367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage17312-030-14557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage17312-030-148af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage17312-030-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage17312-030-141332a3947898…d4bfe170f9cd…

Additional Listing Data#

Finished product
Yes
Brand name base
Heartburn Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACTIVATED CHARCOAL6 [hp_X]/1
POTASSIUM DICHROMATE6 [hp_X]/1
CHELIDONIUM MAJUS6 [hp_X]/1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE6 [hp_X]/1
GINGER6 [hp_X]/1
IRIS VERSICOLOR ROOT6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 6 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2P3VWU3H10Internal UNII lookup
T4423S18FMInternal UNII lookup
7E889U5RNNInternal UNII lookup
70WT22SF4BInternal UNII lookup
C5529G5JPQInternal UNII lookup
X43D4L3DQCInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
14bd30e5-a981-597a-e054-00144ff8d46cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17312-030-142025-11-17C16284748780-1f386c64a-3297-0266-e053-dadaa90a7c1aHeartburn Relief™
17312-030-142023-01-30C16284748780-1f386c64a-3297-0266-e053-dadaa90a7c1aHeartburn Relief™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-030-14Heartburn Relief50 in 1 BOTTLETABLET, ORALLY DISINTEGRATING503
17312-030-14Heartburn Relief1 in 1 PACKAGETABLET, ORALLY DISINTEGRATING13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H10HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNNHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
GINGERACTIVE INGREDIENTC5529G5JPQHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
IRIS VERSICOLOR ROOTACTIVE INGREDIENTX43D4L3DQCHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FMHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATEACTIVE INGREDIENT70WT22SF4BHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H10HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNNHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
DICHROMATE IONACTIVE MOIETY9LKY4BFN2VHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
GINGERACTIVE MOIETYC5529G5JPQHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
IRIS VERSICOLOR ROOTACTIVE MOIETYX43D4L3DQCHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
SODIUM CATIONACTIVE MOIETYLYR4M0NH37HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
COPOVIDONEINACTIVE INGREDIENTD9C330MD8BHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
CROSPOVIDONEINACTIVE INGREDIENT68401960MKHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
MANNITOLINACTIVE INGREDIENT3OWL53L36AHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1
SORBITOLINACTIVE INGREDIENT506T60A25RHEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-030HEARTBURN RELIEF (CARBO MORE) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]2Current NDC, Legacy NDC, 2 package rows20210112_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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Heartburn ReliefCARBO MORETRP Company14bd30e5-a981-597a-e054-00144ff8d46c2025-11-17WarningsExact identifier
ndc (product): 17312-030

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17312-030-14173120030141 BOTTLE in 1 PACKAGE (17312-030-14) / 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE1 bottle2015-04-150000-00-00NoNoCurrent