Oxalis 10% Essence
- Product NDC
- 48951-7160
- 11-digit product format
- 489517160
- Labeler code
- 48951
- Product ID
- 48951-7160_6bb0f068-79a2-face-e053-2a91aa0a7cac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxalis 10% Essence
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- OXALIS STRICTA WHOLE
- Active strength
- 1 [hp_X]/mL
- 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 |
|---|
| 48951-7160-6 | Oxalis 10% Essence | 125 mL in 1 BOTTLE, GLASS | LIQUID | 125 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7160-6 | 48951716006 | 125 mL in 1 BOTTLE, GLASS (48951-7160-6) | 125 ml | 2009-09-01 | 0000-00-00 | No | No | Current |