FDA.reportPublic FDA data

BORAX

Product NDC
60512-6205
11-digit product format
605126205
Labeler code
60512
Product ID
60512-6205_ad394cb5-1035-4263-8251-6bedd29812ac
Type
HUMAN OTC DRUG
Nonproprietary name
BORAX
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
SODIUM BORATE
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-6205-12025-12-30C16284748780-19d75b9d0-b5b7-f424-e053-dadaa90a57ce093a2741-13e0-4db2-b6b2-db64894ce56c
60512-6205-12020-01-31C16284748780-19d75b9d0-b5b7-f424-e053-dadaa90a57ce093a2741-13e0-4db2-b6b2-db64894ce56c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM BORATEACTIVE INGREDIENT91MBZ8H3QOBORAX PELLET [HOMEOLAB USA INC.]1
BORATE IONACTIVE MOIETY44OAE30D22BORAX PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBORAX PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554BORAX PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6205BORAX PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_093a2741-13e0-4db2-b6b2-db64894ce56c.zip