Phosphorus 8

Product NDC
48951-8027
11-digit product format
489518027
Labeler code
48951
Product ID
48951-8027_6d08e600-4beb-4fdf-e053-2991aa0aa78d
Type
HUMAN OTC DRUG
Nonproprietary name
Phosphorus 8
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
PHOSPHORUS
Active strength
8 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Additional Listing Data#

Finished product
Yes
Brand name base
Phosphorus 8
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHOSPHORUS8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
27YLU75U4WInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4efffc9a-f7ca-4b39-822d-e062f789dd19Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8027-1Phosphorus 810 in 1 BOXLIQUID104
48951-8027-1Phosphorus 81 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHOSPHORUSACTIVE INGREDIENT27YLU75U4WPHOSPHORUS 8 LIQUID [URIEL PHARMACY INC.]1
PHOSPHORUSACTIVE MOIETY27YLU75U4WPHOSPHORUS 8 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPHOSPHORUS 8 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPHOSPHORUS 8 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8027PHOSPHORUS 8 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20241027_4efffc9a-f7ca-4b39-822d-e062f789dd19.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
Phosphorus 8PHOSPHORUS 8Uriel Pharmacy Inc.4efffc9a-f7ca-4b39-822d-e062f789dd192026-06-05WarningsExact identifier
ndc (product): 48951-8027

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8027-14895180270110 AMPULE in 1 BOX (48951-8027-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent