Strawberry Sunscreen Lip Moisturizer

Product NDC
75866-306
11-digit product format
758660306
Labeler code
75866
Product ID
75866-306_6e0e43bf-2b0a-49d6-aef1-4a7db3d07ae4
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
75866-306-012019-10-29C16284748780-1960f7f55-db8c-8e05-e053-dbdaa90a074aStrawberry Sunscreen Lip Moisturizer SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75866-306-01Strawberry Sunscreen Lip Moisturizer4.2 g in 1 CONTAINERLIPSTICK4.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75866-306STRAWBERRY SUNSCREEN LIP MOISTURIZER (OCTINOXATE, OXYBENZONE) LIPSTICK [BEACON PROMOTIONS, INC.]1Legacy NDC, 1 package rows20101230_ee5e8872-5c9d-4bd0-bea3-b13b7547e9e7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
75866-306-01758660306014.2 g in 1 CONTAINER4.2 gHistorical