NDC 71741-086 - FolaMax
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71741-086
- Package NDCs from labels
- 71741-086-30
- Manufacturer
- Redmont Pharmaceuticals, LLC
- Effective date
- 2021-11-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FolaMax - Redmont Pharmaceuticals, LLC | Redmont Pharmaceuticals, LLC | 2021-11-22 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71741-086-30 | FolaMax | 30 in 1 BOTTLE | TABLET | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71741-086 | FOLAMAX (BETA CAROTENE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, PYRIDOXINE HYDROCHLORIDE, BIOTIN, FOLIC ACID, LEVOMEFOLATE CALCIUM, CYANOCOBALAMIN, CALCIUM CARBONATE, MAGNESIUM OXIDE, FERROUS BISGLYCINATE, AND POTASSIUM IODIDE) TABLET [REDMONT PHARMACEUTICALS, LLC] | 1 | 1 package rows | 20211123_30cd8d49-ae1e-43ba-b784-778ac2626e9e.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71741-086-30 | EA - Each | 71741-086 | aed17a80-23e6-40aa-8a7b-5c870348bb9f | 1 | 2021-12-08 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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| Soothe childrens | CALCIUM CARBONATE | Walgreen Company | 0235e083-5f3d-4bae-b14a-b12db623180c | 2026-03-31 | Warnings | H0G9379FGK |
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| Equisetum Silicea | EQUISETUM SILICEA | Uriel Pharmacy Inc. | e88b820b-4a07-42e2-8fe2-b30729e91a8c | 2026-03-30 | Warnings | ETJ7Z6XBU4 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.