GUNA OSTEO

Product NDC
17089-473
11-digit product format
170890473
Labeler code
17089
Product ID
17089-473_ba446257-56b6-616f-e053-2a95a90a1f16
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica montana root - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - equisetum hyemale - fumaric acid - SUS SCROFA UMBILICAL CORD - sus scrofa ovary - sus scrofa placenta - comfrey root - succinic acid - silicon dioxide -
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-02-17
Substance
ARNICA MONTANA ROOT; CALCIUM FLUORIDE; CALCIUM PHOSPHATE; COMFREY ROOT; EQUISETUM HYEMALE; FUMARIC ACID; SILICON DIOXIDE; SUCCINIC ACID; SUS SCROFA OVARY; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD
Active strength
3; 8; 8; 6; 3; 4; 8; 4; 6; 6; 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
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA OSTEO
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA ROOT3 [hp_X]/30mL
FUMARIC ACID4 [hp_X]/30mL
SUS SCROFA UMBILICAL CORD6 [hp_X]/30mL
SUS SCROFA OVARY6 [hp_X]/30mL
SUS SCROFA PLACENTA6 [hp_X]/30mL
COMFREY ROOT6 [hp_X]/30mL
SUCCINIC ACID4 [hp_X]/30mL
SILICON DIOXIDE8 [hp_X]/30mL
CALCIUM FLUORIDE8 [hp_X]/30mL
CALCIUM PHOSPHATE8 [hp_X]/30mL
EQUISETUM HYEMALE3 [hp_X]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
MUE8Y11327Internal UNII lookup
88XHZ13131Internal UNII lookup
118OYG6W3HInternal UNII lookup
S7YTV04R8OInternal UNII lookup
C8CV8867O8Internal UNII lookup
M9VVZ08EKQInternal UNII lookup
AB6MNQ6J6LInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
O3B55K4YKIInternal UNII lookup
97Z1WI3NDXInternal UNII lookup
59677RXH25Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
ba4462d6-9751-530f-e053-2995a90a1f16Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-473-18GUNA OSTEO1 in 1 BOXSOLUTION/ DROPS11
17089-473-18GUNA OSTEO30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-473GUNA OSTEO (ARNICA MONTANA ROOT - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - EQUISETUM HYEMALE - FUMARIC ACID - SUS SCROFA UMBILICAL CORD - SUS SCROFA OVARY - SUS SCROFA PLACENTA - COMFREY ROOT - SUCCINIC ACID - SILICON DIOXIDE -) SOLUTION/ DROPS [GUNA SPA]1Current NDC, Legacy NDC, 2 package rows20210217_ba4462d6-9751-530f-e053-2995a90a1f16.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GUNA OSTEOARNICA MONTANA ROOT - CALCIUM FLUORIDE - CALCIUM PHOSPHATE - EQUISETUM HYEMALE - FUMARIC ACID - SUS SCROFA UMBILICAL CORD - SUS SCROFA OVARY - SUS SCROFA PLACENTA - COMFREY ROOT - SUCCINIC ACID - SILICON DIOXIDE -Guna spaba4462d6-9751-530f-e053-2995a90a1f162021-02-17WarningsExact identifier
ndc (product): 17089-473

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-473-18170890473181 BOTTLE, DROPPER in 1 BOX (17089-473-18) / 30 mL in 1 BOTTLE, DROPPER2021-02-170000-00-00NoNoCurrent