Mediflex
- Product NDC
- 67662-001
- 11-digit product format
- 676620001
- Labeler code
- 67662
- Product ID
- 67662-001_286fff75-296a-4268-be96-5b63a797ee41
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- SAS Group Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-03-29
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 5 1/85g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67662-001-03 | Mediflex | 85 g in 1 JAR | CREAM | 85 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67662-001 | MEDIFLEX (MENTHOL) CREAM [SAS GROUP INC.] | 1 | Legacy NDC, 1 package rows | 20100408_d809908d-6ae2-48f2-8325-50d2983ca2ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 67662-001-03 | 67662000103 | 85 g in 1 JAR | 85 g | Historical |