Borax 30C

Product NDC
69152-1071
11-digit product format
691521071
Labeler code
69152
Product ID
69152-1071_2f2ccce2-e113-09ed-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Borax
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-13
Marketing end
0000-00-00
Substance
SODIUM BORATE
Active strength
30 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1071-12020-01-31C16284748780-19d75b9d1-2730-f424-e053-dadaa90a57ce1861e2bb-1be0-1aaa-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1071-1Borax 30C96 in 1 BOTTLEPELLET963

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1071BORAX 30C (BORAX) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]3Legacy NDC, 1 package rows20160329_1861e2bb-1be0-1aaa-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1071-16915210710196 in 1 BOTTLEHistorical