Hepaticol Drops
- Product NDC
- 63083-5008
- 11-digit product format
- 630835008
- Labeler code
- 63083
- Product ID
- 63083-5008_024565f3-cb0f-427b-b0f7-4c9753ddf1d2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hepaticol Drops
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- ATROPINE SULFATE; BEEF LIVER; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS WHOLE; CYSTEINE; GINGER; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CHLORIDE; MILK THISTLE; SODIUM CHLORIDE; SODIUM SULFATE; UBIDECARENONE; VERONICASTRUM VIRGINICUM WHOLE
- Active strength
- 6; 6; 4; 6; 4; 4; 2; 12; 4; 2; 5; 6; 12; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Anticholinergic [EPC], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hepaticol Drops
- Brand name suffix
- 5008
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATROPINE SULFATE | 6 [hp_X]/59mL |
| BEEF LIVER | 6 [hp_X]/59mL |
| BERBERIS VULGARIS ROOT BARK | 4 [hp_X]/59mL |
| BRYONIA ALBA ROOT | 6 [hp_X]/59mL |
| CHELIDONIUM MAJUS WHOLE | 4 [hp_X]/59mL |
| CYSTEINE | 4 [hp_X]/59mL |
| GINGER | 2 [hp_X]/59mL |
| LYCOPODIUM CLAVATUM SPORE | 12 [hp_X]/59mL |
| MAGNESIUM CHLORIDE | 4 [hp_X]/59mL |
| MILK THISTLE | 2 [hp_X]/59mL |
| SODIUM CHLORIDE | 5 [hp_X]/59mL |
| SODIUM SULFATE | 6 [hp_X]/59mL |
| UBIDECARENONE | 12 [hp_X]/59mL |
| VERONICASTRUM VIRGINICUM WHOLE | 3 [hp_X]/59mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 03J5ZE7KA5, W8N8R55022, 1TH8Q20J0U, T7J046YI2B, 7E889U5RNN, K848JZ4886, C5529G5JPQ, C88X29Y479, 02F3473H9O, U946SH95EE, 451W47IQ8X, 0YPR65R21J, EJ27X76M46, 1RA4P35F0I |
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 |
|---|
| 63083-5008-2 | Hepaticol Drops5008 | 59 mL in 1 BOTTLE, DROPPER | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-5008 | HEPATICOL DROPS 5008 (HEPATICOL DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220211_79ee9e37-7853-4560-a87d-cdaefb603bbb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-5008-2 | 63083500802 | 59 mL in 1 BOTTLE, DROPPER (63083-5008-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |