Ultimate Sheer Sunscreen SPF 85

Product NDC
11822-1111
11-digit product format
118221111
Labeler code
11822
Product ID
11822-1111_4bce0359-73b6-479e-9e20-22989bf75725
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3.00% Homosalate 15.00% Octisalate 5.00% Octocrylene 4.50% Oxybenzone 6.00%
Dosage form
LOTION
Route
TOPICAL
Labeler
Ride Aid
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-01-20
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
3 g/100mL; 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
11822-1111-32020-01-31C16284748780-19d75b9d0-3493-f424-e053-dadaa90a57ce4c761bf4-8542-4f8d-a04a-68f9dd2382e2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1111-3Ultimate Sheer Sunscreen SPF 85Rite Aid89 mL in 1 TUBELOTION891

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1111ULTIMATE SHEER SUNSCREEN SPF 85 RITE AID (AVOBENZONE 3.00% HOMOSALATE 15.00% OCTISALATE 5.00% OCTOCRYLENE 4.50% OXYBENZONE 6.00%) LOTION [RIDE AID]1Legacy NDC, 1 package rows20171024_4c761bf4-8542-4f8d-a04a-68f9dd2382e2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
11822-1111-31182211110389 mL in 1 TUBE89 mlHistorical