EB302 ARTHRITIS RELIEF
- Product NDC
- 53304-0302
- 11-digit product format
- 533040302
- Labeler code
- 53304
- Product ID
- 53304-0302_5e6cefe5-d345-4a93-b66b-eec57a2b3091
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- EMINENCE BIOTECH CORPORATION LIMITED
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-11-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 865 mg/50mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 53304-0302-1 | EB302 ARTHRITIS RELIEF | 50 mL in 1 BOTTLE, SPRAY | SPRAY | 50 | | 3 |
| 53304-0302-1 | EB302 ARTHRITIS RELIEF | 1 in 1 BOX | SPRAY | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53304-0302 | EB302 ARTHRITIS RELIEF (MENTHOL) SPRAY [EMINENCE BIOTECH CORPORATION LIMITED] | 3 | Legacy NDC, 2 package rows | 20180321_5230276a-1dcb-4687-a8b8-1221393795e5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53304-0302-1 | 53304030201 | 1 BOTTLE, SPRAY in 1 BOX (53304-0302-1) > 50 mL in 1 BOTTLE, SPRAY | 2012-11-01 | 0000-00-00 | No | No | Current |