FDA.reportPublic FDA data

Drive Sunscreen SPF 50

Product NDC
72667-003
11-digit product format
726670003
Labeler code
72667
Product ID
72667-003_7c5e581f-1992-a172-e053-2a91aa0a27e8
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Humosalate, Octisalate, Octocrylene
Dosage form
SPRAY
Route
TOPICAL
Labeler
Inspec Solutions LLC.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-12-06
Marketing end
0000-00-00
Substance
OCTOCRYLENE; AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
10 g/100mL; g/100mL; g/100mL; g/100mL
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
72667-003-012020-01-31C16284748780-19d75b9d0-988f-f424-e053-dadaa90a57ce7c5e581f-1991-a172-e053-2a91aa0a27e8
72667-003-022020-01-31C16284748780-19d75b9d0-988f-f424-e053-dadaa90a57ce7c5e581f-1991-a172-e053-2a91aa0a27e8
72667-003-032020-01-31C16284748780-19d75b9d0-988f-f424-e053-dadaa90a57ce7c5e581f-1991-a172-e053-2a91aa0a27e8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-003DRIVE SUNSCREEN SPF 50 (AVOBENZONE, HUMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [INSPEC SOLUTIONS LLC.]1Legacy NDC20181208_7c5e581f-1991-a172-e053-2a91aa0a27e8.zip