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

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
CHELIDONIUM MAJUS6 [hp_X]/1
GINGER6 [hp_X]/1
IRIS VERSICOLOR ROOT6 [hp_X]/1
POTASSIUM DICHROMATE6 [hp_X]/1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE6 [hp_X]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii2P3VWU3H10, 7E889U5RNN, C5529G5JPQ, X43D4L3DQC, T4423S18FM, 70WT22SF4B

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

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