NDC 17089-259

OSTEOBIOS

Calcitonin Human - Calcium Carbonate - Calcium Fluoride - Calcium Phosphate - Isoleucine - Leucine - Lysine - Methionine - Phenylalanine - Sus Scrofa Bone - Sus Scrofa Parathyroid Gland - Threonine - Tryptophan - Valine -

OSTEOBIOS is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Calcitonin Human; Isoleucine; Leucine; Lysine; Methionine; Phenylalanine; Threonine; Tryptophan; Valine; Calcium Carbonate; Calcium Fluoride; Calcium Phosphate; Sus Scrofa Bone; Sus Scrofa Parathyroid Gland.

• Product ID: 17089-259_7df35985-5d75-5e35-e053-2a91aa0a033c
• NDC: 17089-259
• Product Type: Human Otc Drug
• Proprietary Name: OSTEOBIOS
• Generic Name: Calcitonin Human - Calcium Carbonate - Calcium Fluoride - Calcium Phosphate - Isoleucine - Leucine - Lysine - Methionine - Phenylalanine - Sus Scrofa Bone - Sus Scrofa Parathyroid Gland - Threonine - Tryptophan - Valine -
• Dosage Form: Solution/ Drops
• Route of Administration: ORAL
• Marketing Start Date: 2006-05-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Guna spa
• Substance Name: CALCITONIN HUMAN; ISOLEUCINE; LEUCINE; LYSINE; METHIONINE; PHENYLALANINE; THREONINE; TRYPTOPHAN; VALINE; CALCIUM CARBONATE; CALCIUM FLUORIDE; CALCIUM PHOSPHATE; SUS SCROFA BONE; SUS SCROFA PARATHYROID GLAND
• Active Ingredient Strength: 6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17089-259-18

1 BOTTLE, DROPPER in 1 BOX (17089-259-18) > 30 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2018-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17089-259-18 [17089025918]

OSTEOBIOS SOLUTION/ DROPS

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-05-01
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-03-13

Drug Details

Active Ingredients

Ingredient	Strength
CALCITONIN HUMAN	6 [hp_X]/30mL

OpenFDA Data

• SPL SET ID: 1b8c8c83-1a46-4c0a-b883-e7dce781c5d1
• Manufacturer:
  • Guna spa
• UNII:
  • 2KBE35NE8S
  • O3B55K4YKI
  • AE28F7PNPL
  • 97Z1WI3NDX
  • 2ZD004190S
  • 47E5O17Y3R
  • K3Z4F929H6
  • I0IO929019
  • 04Y7590D77
  • 597RLJ09RG
  • GMW67QNF9C
  • HG18B9YRS7
  • H0G9379FGK
  • 8DUH1N11BX
• UPC Code:
  • 0317089259183