Diabetic Wound Gel

Product NDC
71521-036
11-digit product format
715210036
Labeler code
71521
Product ID
71521-036_da6fce58-0efb-f3b1-e053-2995a90a1bec
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
GEL
Route
TOPICAL
Labeler
Lavior Inc
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-03-31
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
1 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71521-036-152026-01-29C16284748780-149896155-bed7-586f-e063-e6dba90add90bdc55fbb-e391-0938-e053-2a95a90a1393
71521-036-502026-01-29C16284748780-149896155-bed7-586f-e063-e6dba90add90bdc55fbb-e391-0938-e053-2a95a90a1393

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71521-036DIABETIC WOUND GEL (ALLANTOIN) GEL [LAVIOR PHARMA INC]8Legacy NDC20241025_bdc55fbb-e391-0938-e053-2a95a90a1393.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71521-036-157152100361515 g in 1 TUBE (71521-036-15) 15 g2022-03-170000-00-00NoNoCurrent
71521-036-507152100365050 g in 1 BOTTLE, PUMP (71521-036-50) 50 g2021-03-310000-00-00NoNoCurrent