Cimicifuga Homaccord
- Product NDC
- 50114-1220
- 11-digit product format
- 501141220
- Labeler code
- 50114
- Product ID
- 50114-1220_3d6e9e55-5ae5-4f69-ba6a-57a155791e23
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BLACK COHOSH and STRONTIUM CARBONATE and
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Heel Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1986-01-31
- Marketing end
- 0000-00-00
- Substance
- BLACK COHOSH; STRONTIUM CARBONATE
- Active strength
- 2 [hp_X]/50mL; [hp_X]/50mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50114-1220-4 | Cimicifuga Homaccord | 50 mL in 1 BOTTLE | LIQUID | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50114-1220 | CIMICIFUGA HOMACCORD (BLACK COHOSH AND STRONTIUM CARBONATE AND ) LIQUID [HEEL INC] | 1 | Legacy NDC, 1 package rows | 20120228_6fde5ad7-baf3-460d-a054-83a894a1bb95.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50114-1220-4 | 50114122004 | 50 mL in 1 BOTTLE | 50 ml | Historical |