Amnion 30

Product NDC
48951-1028
11-digit product format
489511028
Labeler code
48951
Product ID
48951-1028_44851bec-6cd0-f3c5-e063-6394a90ade31
Type
HUMAN OTC DRUG
Nonproprietary name
Amnion 30
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
AMNIOTIC FLUID (BOVINE)
Active strength
30 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Amnion 30AMNION 30Uriel Pharmacy Inc.2d63d8f2-db97-43ab-addd-e6be61a66e012025-11-26WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Additional Listing Data#

Finished product
Yes
Brand name base
Amnion 30
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMNIOTIC FLUID (BOVINE)30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiP06X62O7E9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1028-1Amnion 301 mL in 1 AMPULELIQUID15
48951-1028-1Amnion 3010 in 1 BOXLIQUID105

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMNIOTIC FLUID (BOVINE)ACTIVE INGREDIENTP06X62O7E9AMNION 30 LIQUID [URIEL PHARMACY INC.]1
AMNIOTIC FLUID (BOVINE)ACTIVE MOIETYP06X62O7E9AMNION 30 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAMNION 30 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAMNION 30 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1028AMNION 30 LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20241215_2d63d8f2-db97-43ab-addd-e6be61a66e01.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1028-14895110280110 AMPULE in 1 BOX (48951-1028-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent