FDA.reportPublic FDA data

CHOLESTERINUM PLEX

Product NDC
62106-1207
11-digit product format
621061207
Labeler code
62106
Product ID
62106-1207_ed11e5b0-cdb2-1f9a-e053-2995a90a0f16
Type
HUMAN OTC DRUG
Nonproprietary name
Cholesterinum, Cholesterinum, Hepatinum, Pulminum
Dosage form
LIQUID
Route
ORAL
Labeler
Seroyal USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-08-16
Substance
CHOLESTEROL; ORYCTOLAGUS CUNICULUS LIVER; ORYCTOLAGUS CUNICULUS LUNG
Active strength
9; 7; 7 [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CHOLESTERINUM PLEX
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CHOLESTEROL9 [hp_C]/30mL
ORYCTOLAGUS CUNICULUS LIVER7 [hp_C]/30mL
ORYCTOLAGUS CUNICULUS LUNG7 [hp_C]/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii97C5T2UQ7J, 7A99K6361Z, 857C5Q4J3H

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1207-0CHOLESTERINUM PLEX30 mL in 1 BOTTLE, GLASSLIQUID303
62106-1207-0CHOLESTERINUM PLEX1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1207CHOLESTERINUM PLEX (CHOLESTERINUM, CHOLESTERINUM, HEPATINUM, PULMINUM) LIQUID [SEROYAL USA]3Current NDC, Legacy NDC, 2 package rows20221110_56e10d0b-185f-351a-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
62106-1207-0621061207001 BOTTLE, GLASS in 1 CARTON (62106-1207-0) / 30 mL in 1 BOTTLE, GLASS2017-08-160000-00-00NoNoCurrent