Pineapple Sunscreen Lip Moisturizer

Product NDC
75866-305
11-digit product format
758660305
Labeler code
75866
Product ID
75866-305_94cf85f0-6f27-4f43-8912-63b594cbb5d2
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OXYBENZONE
Dosage form
LIPSTICK
Route
TOPICAL
Labeler
Beacon Promotions, Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-12-29
Marketing end
0000-00-00
Substance
OCTINOXATE; OXYBENZONE
Active strength
7 g/100g; g/100g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75866-305-012019-10-29C16284748780-1960f7f55-cc89-8e05-e053-dbdaa90a074aPineapple Sunscreen Lip Moisturizer SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75866-305-01Pineapple Sunscreen Lip Moisturizer4.2 g in 1 CONTAINERLIPSTICK4.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75866-305PINEAPPLE SUNSCREEN LIP MOISTURIZER (OCTINOXATE, OXYBENZONE) LIPSTICK [BEACON PROMOTIONS, INC.]1Legacy NDC, 1 package rows20101230_d55dfda3-c962-4aff-b843-1ce8a6fbe6f1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
75866-305-01758660305014.2 g in 1 CONTAINER4.2 gHistorical