Home NDC 0486-1111 K Phos
Product NDC 0486-1111
11-digit product format 004861111
Labeler code 0486
Product ID 0486-1111_5cdb4128-66e9-4e90-936b-38dd8b5b8688
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Potassium Phosphate, Monobasic
Dosage form TABLET, SOLUBLE
Route ORAL
Labeler Beach Products, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1977-03-29
Substance POTASSIUM PHOSPHATE, MONOBASIC
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base K Phos
Brand name suffix Original
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM PHOSPHATE, MONOBASIC 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4J9FJ0HL51 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1101775 Internal RxNorm lookup 1101778 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0486-1111-01 K PhosOriginal 100 in 1 BOTTLE TABLET, SOLUBLE 100 5 0486-1111-05 K PhosOriginal 500 in 1 BOTTLE TABLET, SOLUBLE 500 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Potassium Phosphate, Monobasic ACTIVE INGREDIENT 4J9FJ0HL51 K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Potassium Cation ACTIVE MOIETY 295O53K152 K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Cellulose, Microcrystalline INACTIVE INGREDIENT OP1R32D61U K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Magnesium Stearate INACTIVE INGREDIENT 70097M6I30 K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Silicon Dioxide INACTIVE INGREDIENT ETJ7Z6XBU4 K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Starch, Corn INACTIVE INGREDIENT O8232NY3SJ K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1 Stearic Acid INACTIVE INGREDIENT 4ELV7Z65AP K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0486-1111 K PHOS ORIGINAL (POTASSIUM PHOSPHATE, MONOBASIC) TABLET, SOLUBLE [BEACH PRODUCTS, INC.] 5 Current NDC, Legacy NDC, 2 package rows 20230302_04557ab3-6d21-49b4-b849-744c75b8a630.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 0486-1111-01 00486111101 100 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-01) 1977-03-29 0000-00-00 No No Current 0486-1111-05 00486111105 500 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-05) 1977-03-29 0000-00-00 No No Current