Kalium aceticum comp. 6

Product NDC
48951-6004
11-digit product format
489516004
Labeler code
48951
Product ID
48951-6004_6ac65534-fa20-379f-e053-2991aa0a3955
Type
HUMAN OTC DRUG
Nonproprietary name
Kalium aceticum comp. 6
Dosage form
POWDER
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CORALLIUM RUBRUM EXOSKELETON; SAFFRON; POTASSIUM ACETATE; ANTIMONY TRISULFIDE
Active strength
6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
2CA71K0DLECORALLIUM RUBRUM EXOSKELETONCORALLIUM RUBRUM EXOSKELETON
E849G4X5YJSAFFRONSAFFRON
M911911U02POTASSIUM ACETATE127-08-2POTASSIUM ACETATE
F79059A38UANTIMONY TRISULFIDE1345-04-6ANTIMONY TRISULFIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-6004-44895160040450 g in 1 BOTTLE, GLASS (48951-6004-4) 50 g2009-09-010000-00-00NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Kalium aceticum comp. 6Uriel Pharmacy Inc.2024-12-11HUMAN OTC DRUG LABEL6