Kalium Sulfuratum Bath Essence

Product NDC
48951-6071
11-digit product format
489516071
Labeler code
48951
Product ID
48951-6071_6ba0600c-03c3-e39b-e053-2a91aa0a6234
Type
HUMAN OTC DRUG
Nonproprietary name
Kalium Sulfuratum Bath Essence
Dosage form
LIQUID
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SULFUR
Active strength
1 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-6071-6Kalium Sulfuratum Bath Essence125 mL in 1 BOTTLE, GLASSLIQUID1252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-6071KALIUM SULFURATUM BATH ESSENCE LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240207_6ba0600c-03c2-e39b-e053-2a91aa0a6234.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-6071-648951607106125 mL in 1 BOTTLE, GLASS (48951-6071-6) 125 ml2009-09-010000-00-00NoNoCurrent