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

Harmonized Identifiers#

Field, Values table
FieldValues
UniiDIF093I037, C0ZK0RRF5X, 49OY13BE7Z, 27YLU75U4W, 1Z00ZK3E66

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

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