Ultra Strength Pain Relief
- Product NDC
- 64048-5114
- 11-digit product format
- 640485114
- Labeler code
- 64048
- Product ID
- 64048-5114_2c4c25cc-4283-435e-a614-1cad8d1338f6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor 4%, Menthol 10%, Methyl Salicylate 30%
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Product Quest Mfg
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-02-06
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
- Active strength
- 4 g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 64048-5114-4 | Ultra Strength Pain Relief | 113 g in 1 CAN | SPRAY | 113 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64048-5114 | ULTRA STRENGTH PAIN RELIEF (CAMPHOR 4%, MENTHOL 10%, METHYL SALICYLATE 30%) SPRAY [PRODUCT QUEST MFG] | 1 | Legacy NDC, 1 package rows | 20180625_4a595401-20af-437e-a658-44e9358d9008.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 64048-5114-4 | 64048511404 | 113 g in 1 CAN | 113 g | Historical |