Oxalis 20
- Product NDC
- 48951-7180
- 11-digit product format
- 489517180
- Labeler code
- 48951
- Product ID
- 48951-7180_81404737-8f10-6dce-e053-2a91aa0a1478
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis 20
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- OXALIS ACETOSELLA LEAF
- Active strength
- 1 [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 |
|---|
| 48951-7180-5 | Oxalis 20 | 60 g in 1 TUBE | GEL | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7180 | OXALIS 20 GEL [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20190213_81404737-8f0f-6dce-e053-2a91aa0a1478.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7180-5 | 48951718005 | 60 g in 1 TUBE (48951-7180-5) | 60 g | 2009-09-01 | 0000-00-00 | No | No | Current |