Fibro Flex
- Product NDC
- 61495-401
- 11-digit product format
- 614950401
- Labeler code
- 61495
- Product ID
- 61495-401_bb010f87-cfad-4deb-b8d3-bcefdf4f58ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesia Muriatica
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- MAGNESIUM DIRECT INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-11
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM CHLORIDE
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 61495-401-04 | Fibro Flex | 118 mL in 1 BOTTLE | SPRAY | 118 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61495-401 | FIBRO FLEX (MAGNESIA MURIATICA) SPRAY [MAGNESIUM DIRECT INC.] | 1 | Legacy NDC, 1 package rows | 20150721_be87ed5a-9cd3-423c-bee3-ac7207d6b9ec.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 61495-401-04 | 61495040104 | 118 mL in 1 BOTTLE | 118 ml | Historical |