Rheum Combination
- Product NDC
- 63083-9240
- 11-digit product format
- 630839240
- Labeler code
- 63083
- Product ID
- 63083-9240_b89d688f-e7f1-49a1-b55e-c193d2adfd7b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Rheum Combination
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- ALOE; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; FRANGULA ALNUS BARK; GRAPHITE; MEDICAGO SATIVA WHOLE; RHEUM OFFICINALE STEM; SENNA LEAF; STAR ANISE; STRYCHNOS NUX-VOMICA SEED; VERONICASTRUM VIRGINICUM WHOLE
- Active strength
- 4; 4; 6; 2; 8; 1; 1; 1; 1; 4; 1 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rheum Combination
- Brand name suffix
- 9240
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALOE | 4 [hp_X]/29.5mL |
| BRYONIA ALBA ROOT | 4 [hp_X]/29.5mL |
| CITRULLUS COLOCYNTHIS FRUIT PULP | 6 [hp_X]/29.5mL |
| FRANGULA ALNUS BARK | 2 [hp_X]/29.5mL |
| GRAPHITE | 8 [hp_X]/29.5mL |
| MEDICAGO SATIVA WHOLE | 1 [hp_X]/29.5mL |
| RHEUM OFFICINALE STEM | 1 [hp_X]/29.5mL |
| SENNA LEAF | 1 [hp_X]/29.5mL |
| STAR ANISE | 1 [hp_X]/29.5mL |
| STRYCHNOS NUX-VOMICA SEED | 4 [hp_X]/29.5mL |
| VERONICASTRUM VIRGINICUM WHOLE | 1 [hp_X]/29.5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V5VD430YW9, T7J046YI2B, 23H32AOH17, S2D77IH61R, 4QQN74LH4O, DJO934BRBD, 82X32CRA5U, AK7JF626KX, XKC1657P78, 269XH13919, 1RA4P35F0I |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63083-9240-1 | Rheum Combination9240 | 29.5 mL in 1 BOTTLE, DROPPER | LIQUID | 29.5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-9240 | RHEUM COMBINATION 9240 (RHEUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220210_f65a41b7-5931-4c62-89a3-7b255757527f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-9240-1 | 63083924001 | 29.5 mL in 1 BOTTLE, DROPPER (63083-9240-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |