Amber Amethyst
- Product NDC
- 48951-1270
- 11-digit product format
- 489511270
- Labeler code
- 48951
- Product ID
- 48951-1270_7cc2ff8e-b639-b8d6-e053-2a91aa0a2b87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Amber Amethyst
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- HORSE CHESTNUT; EQUISETUM ARVENSE TOP; AMBER; SILICON DIOXIDE
- Active strength
- 2 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1270-5 | Amber Amethyst | 60 g in 1 TUBE | CREAM | 60 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1270 | AMBER AMETHYST CREAM [URIEL PHARMACY INC.] | 4 | Legacy NDC, 1 package rows | 20241207_8f0cebad-895e-494d-9112-a0a8ab09ea44.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1270-5 | 48951127005 | 60 g in 1 TUBE (48951-1270-5) | 60 g | 2009-09-01 | 0000-00-00 | No | No | Current |