Aletris Combination
- Product NDC
- 63083-9203
- 11-digit product format
- 630839203
- Labeler code
- 63083
- Product ID
- 63083-9203_eb4d236e-99a3-435e-b20b-b13d8b1f5086
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aletris Combination
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- ALETRIS FARINOSA ROOT; ANAMIRTA COCCULUS FRUIT; CHAMAELIRIUM LUTEUM ROOT; FERRIC CATION; FERROSOFERRIC PHOSPHATE; FERROUS CATION; IRON; PICRIC ACID; POTASSIUM CARBONATE; QUININE ARSENITE; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE
- Active strength
- 4; 4; 6; 6; 6; 6; 6; 6; 8; 8; 6; 6 [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; [hp_X]/29.5mL
- Pharmacologic classes
- Antimalarial [EPC], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aletris Combination
- Brand name suffix
- 9203
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALETRIS FARINOSA ROOT | 4 [hp_X]/29.5mL |
| ANAMIRTA COCCULUS FRUIT | 4 [hp_X]/29.5mL |
| CHAMAELIRIUM LUTEUM ROOT | 6 [hp_X]/29.5mL |
| FERRIC CATION | 6 [hp_X]/29.5mL |
| FERROSOFERRIC PHOSPHATE | 6 [hp_X]/29.5mL |
| FERROUS CATION | 6 [hp_X]/29.5mL |
| IRON | 6 [hp_X]/29.5mL |
| PICRIC ACID | 6 [hp_X]/29.5mL |
| POTASSIUM CARBONATE | 8 [hp_X]/29.5mL |
| QUININE ARSENITE | 8 [hp_X]/29.5mL |
| SEPIA OFFICINALIS JUICE | 6 [hp_X]/29.5mL |
| SODIUM CHLORIDE | 6 [hp_X]/29.5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O021JGR97X, 3E8XBL6YYK, DQV54Y5H3U, 91O4LML611, 91GQH8I5F7, GW89581OWR, E1UOL152H7, A49OS0F91S, BQN1B9B9HA, 42QO5P0NLM, QDL83WN8C2, 451W47IQ8X |
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 |
|---|
| 63083-9203-1 | Aletris Combination9203 | 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 |
|---|
| 63083-9203 | ALETRIS COMBINATION 9203 (ALETRIS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220210_87ae7310-927b-48fe-b659-6f93dad62363.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-9203-1 | 63083920301 | 29.5 mL in 1 BOTTLE, DROPPER (63083-9203-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |