DEARDERM DAILY MOSITURE SUNSCREEN

Product NDC
72279-078
11-digit product format
722790078
Labeler code
72279
Product ID
72279-078_496ec7c6-8122-405a-9470-a930e4e7d7bd
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
RAINBOW BEAUTY COMPANY
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-06-01
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72279-078-012022-01-28C16284748780-1d6a99b39-eda2-a426-e053-dadaa90af4c2DEARDERM DAILY MOISTURE SUNSCREEN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72279-078-01DEARDERM DAILY MOSITURE SUNSCREEN88 mL in 1 TUBELOTION882

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72279-078DEARDERM DAILY MOSITURE SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [RAINBOW BEAUTY COMPANY]2Legacy NDC, 1 package rows20200123_a647eab1-200a-497d-8bee-72a65729fdb8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72279-078-017227900780188 mL in 1 TUBE (72279-078-01) 88 ml2018-06-010000-00-00NoNoCurrent