LIGHT CARE AQUA SUN

Product NDC
69894-100
11-digit product format
698940100
Labeler code
69894
Product ID
69894-100_32495787-4fc4-40e9-8729-ff4c52eeafce
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Octocrylene, Octisalate, Avobenzone
Dosage form
GEL
Route
TOPICAL
Labeler
WOW VENTURES
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-05-01
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Active strength
4 mg/50mL; mg/50mL; mg/50mL; mg/50mL
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
69894-100-012020-01-31C16284748780-19d75b9d0-9f3d-f424-e053-dadaa90a57ceae28ea61-b1f4-451c-b439-551f05bda0a7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69894-100-01LIGHT CARE AQUA SUN50 mL in 1 CARTONGEL501

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69894-100LIGHT CARE AQUA SUN (OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) GEL [WOW VENTURES]1Legacy NDC, 1 package rows20150624_ae28ea61-b1f4-451c-b439-551f05bda0a7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69894-100-016989401000150 mL in 1 CARTON50 mlHistorical