Osteodoron AM Special Formula

Product NDC
48951-7115
11-digit product format
489517115
Labeler code
48951
Product ID
48951-7115_6ad9967f-be68-1066-e053-2a91aa0abd95
Type
HUMAN OTC DRUG
Nonproprietary name
Osteodoron AM 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
CUCURBITA PEPO FLOWER; FLUORAPATITE; CALCIUM FLUORIDE; SILICON DIOXIDE; LEAD CARBONATE
Active strength
3 [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
413MGP37HQCUCURBITA PEPO FLOWERCUCURBITA PEPO FLOWER
M4CM1H238JFLUORAPATITE1306-05-4FLUORAPATITE
O3B55K4YKICALCIUM FLUORIDE7789-75-5CALCIUM FLUORIDE
ETJ7Z6XBU4SILICON DIOXIDE7631-86-9SILICON DIOXIDE
43M0P24L2BLEAD CARBONATE598-63-0LEAD CARBONATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7115-44895171150460 g in 1 BOTTLE, GLASS (48951-7115-4) 60 g2009-09-010000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Osteodoron AM Special FormulaUriel Pharmacy Inc.2018-04-27HUMAN OTC DRUG LABEL3