FDA.reportPublic FDA data

Cartilago Argentum

Product NDC
48951-3260
11-digit product format
489513260
Labeler code
48951
Product ID
48951-3260_43e57be5-d1f4-b1c8-e063-6394a90ac681
Type
HUMAN OTC DRUG
Nonproprietary name
Cartilago Argentum
Dosage form
CREAM
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ACONITUM NAPELLUS; ANTIMONY TRISULFIDE; ARNICA MONTANA; BETULA PUBESCENS LEAF; BOS TAURUS CARTILAGE; MANDRAGORA OFFICINARUM ROOT; SILVER
Active strength
6; 5; 6; 3; 8; 3; 8 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cartilago Argentum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS6 [hp_X]/g
ANTIMONY TRISULFIDE5 [hp_X]/g
ARNICA MONTANA6 [hp_X]/g
BETULA PUBESCENS LEAF3 [hp_X]/g
BOS TAURUS CARTILAGE8 [hp_X]/g
MANDRAGORA OFFICINARUM ROOT3 [hp_X]/g
SILVER8 [hp_X]/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, F79059A38U, O80TY208ZW, 84SOH0O3OO, UE77B10IIY, I2XCB174VB, 3M4G523W1G

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3260-5Cartilago Argentum60 g in 1 TUBECREAM604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3260CARTILAGO ARGENTUM CREAM [URIEL PHARMACY INC.]3Current NDC, 1 package rows20241206_0f3bf8ce-0a60-4a79-e063-6294a90a3932.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-3260-54895132600560 g in 1 TUBE (48951-3260-5) 60 g2009-09-01NoNoCurrent