BEACH DREAM GLITTERY SUNSCREEN

Product NDC
76853-102
11-digit product format
768530102
Labeler code
76853
Product ID
76853-102_aa102f68-2104-4d6b-ae3f-ae9a30a23003
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
Block LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-08-23
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3 g/100mL; g/100mL; g/100mL; g/100mL
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
76853-102-112023-01-30C16284748780-1f386c649-e46b-0266-e053-dadaa90a7c1aBEACH DREAM GLITTERY SUNSCREEN SPF 30
76853-102-122023-01-30C16284748780-1f386c649-e46b-0266-e053-dadaa90a7c1aBEACH DREAM GLITTERY SUNSCREEN SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76853-102-11BEACH DREAM GLITTERY SUNSCREENSPF 3090 mL in 1 TUBELOTION903
76853-102-12BEACH DREAM GLITTERY SUNSCREENSPF 30180 mL in 1 TUBELOTION1803

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76853-102BEACH DREAM GLITTERY SUNSCREEN SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BLOCK LLC]3Legacy NDC, 2 package rows20200824_fefd6d0b-88a5-4218-a6df-c4a733aaf3e6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76853-102-117685301021190 mL in 1 TUBE (76853-102-11) 90 ml2020-08-230000-00-00NoNoCurrent
76853-102-1276853010212180 mL in 1 TUBE (76853-102-12) 180 ml2020-08-230000-00-00NoNoCurrent