Amnion Oxalis comp.
- Product NDC
- 48951-1396
- 11-digit product format
- 489511396
- Labeler code
- 48951
- Product ID
- 48951-1396_2d7f3585-002c-854b-e063-6294a90ab9fa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Amnion Oxalis comp.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- AMNIOTIC FLUID (BOVINE); KALANCHOE DAIGREMONTIANA LEAF; OXALIS STRICTA WHOLE
- Active strength
- 30; 3; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amnion Oxalis comp.
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMNIOTIC FLUID (BOVINE) | 30 [hp_X]/mL |
| KALANCHOE DAIGREMONTIANA LEAF | 3 [hp_X]/mL |
| OXALIS STRICTA WHOLE | 3 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | P06X62O7E9, L6X13JKL8O, 3STW243384 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1396-3 | Amnion Oxalis comp. | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1396 | AMNION OXALIS COMP. LIQUID [URIEL PHARMACY, INC] | 1 | Current NDC, 1 package rows | 20250210_2d7f3585-002b-854b-e063-6294a90ab9fa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-1396-3 | 48951139603 | 60 mL in 1 BOTTLE, DROPPER (48951-1396-3) | 60 ml | 2009-09-01 | No | No | Current |