Sea and Ski SPF 50 Sport

Product NDC
73440-2082
11-digit product format
734402082
Labeler code
73440
Product ID
73440-2082_be747cba-5727-9495-e053-2a95a90a6229
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone,Homosalate,Octinoxate,Octisalate,Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Cross-Brands Contract Filling
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-02-01
Marketing end
0000-00-00
Substance
OCTOCRYLENE; AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE
Active strength
12 g/237g; g/237g; g/237g; g/237g; g/237g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73440-2082-12023-01-30C16284748780-1f386c649-ab7a-0266-e053-dadaa90a7c1aSea & Ski SPF 50 Sport Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73440-2082-1Sea and Ski SPF 50 Sport237 g in 1 TUBELOTION2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73440-2082SEA AND SKI SPF 50 SPORT (AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE,OCTOCRYLENE) LOTION [CROSS-BRANDS CONTRACT FILLING]1Legacy NDC, 1 package rows20210327_be747cba-5724-9495-e053-2a95a90a6229.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73440-2082-173440208201237 g in 1 TUBE (73440-2082-1) 237 g2017-02-010000-00-00NoNoCurrent