Home FDA labels 2b9efed7-5d8a-16bd-e063-6394a90ac14f D-133 openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name D-133
Generic name CALCIUM FLUORIDE, SILICON DIOXIDE, TRIBASIC CALCIUM PHOSPHATE, CALCIUM SULFATE ANHYDROUS, FERROSOFERRIC PHOSPHATE, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, POTASSIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM CHLORIDE, AND SODIUM SULFATE
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID a250b7e9-7fd2-4cb0-82f3-baa089d17441
SPL ID 2b9efed7-5d8a-16bd-e063-6394a90ac14f
Version 3
Effective date 2025-01-13
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:57 Harmonized routes table Harmonized routes SUBLINGUAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D-133 openfda.brand_name generic name CALCIUM FLUORIDE, SILICON DIOXIDE, TRIBASIC CALCIUM PHOSPHATE, CALCIUM SULFATE ANHYDROUS, FERROSOFERRIC PHOSPHATE, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, POTASSIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM CHLORIDE, AND SODIUM SULFATE openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0139-1 openfda.package_ndc ndc product 58264-0139 openfda.product_ndc ndc11 package 58264013901 derived:openfda.package_ndc spl id 2b9efed7-5d8a-16bd-e063-6394a90ac14f id spl set id a250b7e9-7fd2-4cb0-82f3-baa089d17441 set_id unii E934B3V59H openfda.unii unii CI71S98N1Z openfda.unii unii O3B55K4YKI openfda.unii unii 0YPR65R21J openfda.unii unii 91D9GV0Z28 openfda.unii unii HF539G9L3Q openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii 91GQH8I5F7 openfda.unii unii 1K573LC5TV openfda.unii unii 660YQ98I10 openfda.unii unii 70WT22SF4B openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.