Osteodoron PM Special Formula

Product NDC
48951-7161
11-digit product format
489517161
Labeler code
48951
Product ID
48951-7161_6bb1d864-6349-6b0c-e053-2991aa0ab4c9
Type
HUMAN OTC DRUG
Nonproprietary name
Osteodoron PM Special Formula
Dosage form
POWDER
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CALCIUM FLUORIDE; SILICON DIOXIDE; LEAD CARBONATE; OSTREA EDULIS SHELL; QUERCUS ROBUR WHOLE
Active strength
6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
O3B55K4YKICALCIUM FLUORIDE7789-75-5CALCIUM FLUORIDE
ETJ7Z6XBU4SILICON DIOXIDE7631-86-9SILICON DIOXIDE
43M0P24L2BLEAD CARBONATE598-63-0LEAD CARBONATE
49OY13BE7ZOSTREA EDULIS SHELLOSTREA EDULIS SHELL
R7QMG0BT2WQUERCUS ROBUR WHOLEQUERCUS ROBUR WHOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7161-44895171610450 g in 1 BOTTLE, GLASS (48951-7161-4) 50 g2009-09-010000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Osteodoron PM Special FormulaUriel Pharmacy Inc.2024-01-17HUMAN OTC DRUG LABEL2