Agaricus Phosphorus

Product NDC
48951-1022
11-digit product format
489511022
Labeler code
48951
Product ID
48951-1022_44210514-6a82-7a7f-e063-6394a90ae413
Type
HUMAN OTC DRUG
Nonproprietary name
Agaricus Phosphorus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
AMANITA MUSCARIA FRUITING BODY; DRYOPTERIS FILIX-MAS ROOT; OSTREA EDULIS SHELL; PHOSPHORUS; SILVER FLUORIDE
Active strength
8; 3; 6; 6; 6 [hp_X]/mL; [hp_X]/mL; [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
Agaricus Phosphorus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DRYOPTERIS FILIX-MAS ROOT3 [hp_X]/mL
SILVER FLUORIDE6 [hp_X]/mL
OSTREA EDULIS SHELL6 [hp_X]/mL
PHOSPHORUS6 [hp_X]/mL
AMANITA MUSCARIA FRUITING BODY8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
C0ZK0RRF5XInternal UNII lookup
1Z00ZK3E66Internal UNII lookup
49OY13BE7ZInternal UNII lookup
27YLU75U4WInternal UNII lookup
DIF093I037Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
b6431e0b-6d84-423f-a1be-6701aa848f8dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1022-1Agaricus Phosphorus10 in 1 BOXLIQUID106
48951-1022-1Agaricus Phosphorus1 mL in 1 AMPULELIQUID16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AMANITA MUSCARIA FRUITING BODYACTIVE INGREDIENTDIF093I037AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
DRYOPTERIS FILIX-MAS ROOTACTIVE INGREDIENTC0ZK0RRF5XAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
OSTREA EDULIS SHELLACTIVE INGREDIENT49OY13BE7ZAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4WAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
SILVER FLUORIDEACTIVE INGREDIENT1Z00ZK3E66AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
AMANITA MUSCARIA FRUITING BODYACTIVE MOIETYDIF093I037AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
DRYOPTERIS FILIX-MAS ROOTACTIVE MOIETYC0ZK0RRF5XAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
OSTREA EDULIS SHELLACTIVE MOIETY49OY13BE7ZAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
PHOSPHORUSACTIVE MOIETY27YLU75U4WAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
SILVER FLUORIDEACTIVE MOIETY1Z00ZK3E66AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RAGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1022AGARICUS PHOSPHORUS LIQUID [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 2 package rows20241207_b6431e0b-6d84-423f-a1be-6701aa848f8d.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
Agaricus PhosphorusAGARICUS PHOSPHORUSUriel Pharmacy Inc.b6431e0b-6d84-423f-a1be-6701aa848f8d2025-11-21WarningsExact identifier
ndc (product): 48951-1022

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1022-14895110220110 AMPULE in 1 BOX (48951-1022-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent