Phosphorus 6

Product NDC
48951-8026
11-digit product format
489518026
Labeler code
48951
Product ID
48951-8026_6b10d657-8e9e-2222-e053-2a91aa0a654f
Type
HUMAN OTC DRUG
Nonproprietary name
Phosphorus 6
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
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8026-3Phosphorus 660 mL in 1 BOTTLE, DROPPERLIQUID604

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHOSPHORUSACTIVE INGREDIENT27YLU75U4WPHOSPHORUS 6 LIQUID [URIEL PHARMACY INC.]1
PHOSPHORUSACTIVE MOIETY27YLU75U4WPHOSPHORUS 6 LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MPHOSPHORUS 6 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPHOSPHORUS 6 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8026PHOSPHORUS 6 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20241027_efc10d71-fcea-4c72-951d-15fa00e06f3f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8026-34895180260360 mL in 1 BOTTLE, DROPPER (48951-8026-3) 60 ml2009-09-010000-00-00NoNoCurrent