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
KALANCHOE DAIGREMONTIANA LEAF; AMNIOTIC FLUID (BOVINE); OXALIS STRICTA WHOLE
Active strength
3; 30; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Amnion Oxalis comp.
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
KALANCHOE DAIGREMONTIANA LEAF3 [hp_X]/mL
AMNIOTIC FLUID (BOVINE)30 [hp_X]/mL
OXALIS STRICTA WHOLE3 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
L6X13JKL8OInternal UNII lookup
P06X62O7E9Internal UNII lookup
3STW243384Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2d7f3585-002b-854b-e063-6294a90ab9faAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1396-3Amnion Oxalis comp.60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1396AMNION OXALIS COMP. LIQUID [URIEL PHARMACY, INC]1Current NDC, 1 package rows20250210_2d7f3585-002b-854b-e063-6294a90ab9fa.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Amnion Oxalis comp.AMNION OXALIS COMP.Uriel Pharmacy, Inc2d7f3585-002b-854b-e063-6294a90ab9fa2025-02-06WarningsExact identifier
ndc (product): 48951-1396

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-1396-34895113960360 mL in 1 BOTTLE, DROPPER (48951-1396-3) 60 ml2009-09-01NoNoCurrent