Gentle Therapy Treatment

Product NDC
71693-101
11-digit product format
716930101
Labeler code
71693
Product ID
71693-101_57dae7c8-cc2d-1c65-e053-2991aa0ac58a
Type
HUMAN OTC DRUG
Nonproprietary name
Panthenol
Dosage form
LIQUID
Route
TOPICAL
Labeler
SOLEO
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-08-28
Marketing end
0000-00-00
Substance
PANTHENOL
Active strength
4 g/750mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71693-101-022020-11-13C16284748780-19d75b9d0-8daf-f424-e053-dadaa90a57ce57dae7c8-cc2c-1c65-e053-2991aa0ac58a
71693-101-022020-01-31C16284748780-19d75b9d0-8daf-f424-e053-dadaa90a57ce57dae7c8-cc2c-1c65-e053-2991aa0ac58a