Unishield Back Pain Relief
- Product NDC
- 49314-0748
- 11-digit product format
- 493140748
- Labeler code
- 49314
- Product ID
- 49314-0748_e82afa5e-41be-2959-e053-2a95a90a07de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesium salicylate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unishield
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-09-26
- Marketing end
- 0000-00-00
- Substance
- MAGNESIUM SALICYLATE
- Active strength
- 580 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49314-0748-0 | Unishield Back Pain Relief | 40 in 1 BOX | TABLET, FILM COATED | 40 | | 3 |
| 49314-0748-0 | Unishield Back Pain Relief | 2 in 1 PACKET | TABLET, FILM COATED | 2 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49314-0748 | UNISHIELD BACK PAIN RELIEF (MAGNESIUM SALICYLATE) TABLET, FILM COATED [UNISHIELD] | 3 | Legacy NDC, 2 package rows | 20240118_e56e6162-4c3f-5e68-e053-2a95a90a9c74.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49314-0748-0 | 49314074800 | 40 PACKET in 1 BOX (49314-0748-0) > 2 TABLET, FILM COATED in 1 PACKET | 40 packet | 2022-09-26 | 0000-00-00 | No | No | Current |