Silagen

Product NDC
69291-6230
11-digit product format
692916230
Labeler code
69291
Product ID
69291-6230_edc1aa3e-348f-0a6b-e053-2a95a90ab858
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide, Sunscreen
Dosage form
GEL
Route
TOPICAL
Labeler
NewMedical Technology Inc.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-06-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
20 g/100g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69291-6230-1Silagen1 in 1 CARTONGEL19
69291-6230-2Silagen30 g in 1 BOTTLE, PUMPGEL309

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69291-6230SILAGEN (ZINC OXIDE, SUNSCREEN) GEL [NEWMEDICAL TECHNOLOGY INC.]9Legacy NDC, 2 package rows20230609_486c44cd-47b3-537d-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69291-6230-1692916230011 BOTTLE, PUMP in 1 CARTON (69291-6230-1) > 30 g in 1 BOTTLE, PUMP (69291-6230-2) 2015-06-010000-00-00NoNoCurrent
69291-6230-26929162300230 g in 1 BOTTLE, PUMP30 gHistorical