FDA.reportPublic FDA data

Mercurialis Calendula DKS

Product NDC
48951-7223
11-digit product format
489517223
Labeler code
48951
Product ID
48951-7223_43f8dcdb-1cc2-7f1d-e063-6394a90ad1b6
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurialis Calendula DKS
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ANTIMONY; CALENDULA OFFICINALIS FLOWERING TOP; GOLD; MERCURIALIS PERENNIS; ONION; URTICA DIOICA
Active strength
8; 1; 8; 1; 1; 8 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Mercurialis Calendula DKS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MERCURIALIS PERENNIS8 [hp_X]/g
CALENDULA OFFICINALIS FLOWERING TOP1 [hp_X]/g
GOLD8 [hp_X]/g
ANTIMONY1 [hp_X]/g
URTICA DIOICA1 [hp_X]/g
ONION8 [hp_X]/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQ35465A1MA, 18E7415PXQ, 79Y1949PYO, 9IT35J3UV3, 710FLW4U46, 492225Q21H

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7223-5Mercurialis Calendula DKS60 g in 1 TUBEOINTMENT602

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-7223-54895172230560 g in 1 TUBE (48951-7223-5) 60 g2009-09-01NoNoCurrent