FDA.reportPublic FDA data

ACETALDEHYDE

Product NDC
60512-6152
11-digit product format
605126152
Labeler code
60512
Product ID
60512-6152_b67a6747-5ec3-4c79-9768-13c45b1bbc21
Type
HUMAN OTC DRUG
Nonproprietary name
ACETALDEHYDE
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ACETALDEHYDE
Active strength
6 [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
60512-6152-12025-12-26C16284748780-19d75b9d0-b044-f424-e053-dadaa90a57ce68bdf7c5-20b7-4f88-a54f-369ede201bdf
60512-6152-12020-01-31C16284748780-19d75b9d0-b044-f424-e053-dadaa90a57ce68bdf7c5-20b7-4f88-a54f-369ede201bdf

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETALDEHYDEACTIVE INGREDIENTGO1N1ZPR3BACETALDEHYDE PELLET [HOMEOLAB USA INC.]1
ACETALDEHYDEACTIVE MOIETYGO1N1ZPR3BACETALDEHYDE PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACETALDEHYDE PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ACETALDEHYDE PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6152ACETALDEHYDE PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_68bdf7c5-20b7-4f88-a54f-369ede201bdf.zip