Sambucus comp.

Product NDC
48951-8435
11-digit product format
489518435
Labeler code
48951
Product ID
48951-8435_36ea2222-8edc-156d-e063-6394a90a2866
Type
HUMAN OTC DRUG
Nonproprietary name
Sambucus comp.
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
BERBERIS VULGARIS ROOT BARK; PHOSPHORUS; SAMBUCUS NIGRA FLOWERING TOP; TEUCRIUM SCORODONIA WHOLE
Active strength
6; 6; 3; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sambucus comp.
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SAMBUCUS NIGRA FLOWERING TOP6 [hp_X]/mL
TEUCRIUM SCORODONIA WHOLE6 [hp_X]/mL
BERBERIS VULGARIS ROOT BARK3 [hp_X]/mL
PHOSPHORUS4 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiCT03BSA18U, 2MJ724W91Q, 1TH8Q20J0U, 27YLU75U4W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8435-3Sambucus comp.60 mL in 1 BOTTLE, DROPPERLIQUID601

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-8435-34895184350360 mL in 1 BOTTLE, DROPPER (48951-8435-3) 60 ml2009-09-01NoNoHistorical