Derma Soleil Dry Sport SPF 30

Product NDC
69711-308
11-digit product format
697110308
Labeler code
69711
Product ID
69711-308_55135e2c-52e9-3e36-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Octocrylene, Octyl Methoxycinnamate, Octyl Salicylate, Oxybenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
Derma Soleil
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-07-20
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE
Active strength
8 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69711-308-012020-01-31C16284748780-19d75b9d0-5f71-f424-e053-dadaa90a57ceDerma Soleil Dry Sport SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69711-308-01Derma Soleil Dry Sport SPF 30120 mL in 1 BOTTLE, SPRAYLOTION1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69711-308DERMA SOLEIL DRY SPORT SPF 30 (OCTOCRYLENE, OCTYL METHOXYCINNAMATE, OCTYL SALICYLATE, OXYBENZONE) LOTION [DERMA SOLEIL]1Legacy NDC, 1 package rows20170724_55135e2c-52e8-3e36-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69711-308-0169711030801120 mL in 1 BOTTLE, SPRAY120 mlHistorical