All Day Skin Relief with Colloidal Oats

Product NDC
50154-012
11-digit product format
501540012
Labeler code
50154
Product ID
50154-012_32c041a6-afee-461b-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
CETYL ALCOHOL
Dosage form
LOTION
Route
TOPICAL
Labeler
Lantern Enterprises Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-05-13
Marketing end
0000-00-00
Substance
CETYL ALCOHOL
Active strength
80 mg/100mL
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
50154-012-502021-10-31C16284748780-19d75b9d0-6cca-f424-e053-dadaa90a57ce31e07369-e63e-439c-e054-00144ff88e88
50154-012-502020-01-31C16284748780-19d75b9d0-6cca-f424-e053-dadaa90a57ce31e07369-e63e-439c-e054-00144ff88e88