COOLA Classic Body Sunscreen Guava Mango

Product NDC
21839-450
11-digit product format
218390450
Labeler code
21839
Product ID
21839-450_9aa24411-fdae-c256-e053-2a95a90a3649
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE,HOMOSALATE, OCTISALATE,OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
Gordon Laboratories, Inc.
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-01-31
Marketing end
0000-00-00
Substance
AVOBENZONE; OCTISALATE; OCTOCRYLENE; HOMOSALATE
Active strength
18 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21839-450-022021-01-29C16284748780-1ba0f9c33-213e-a910-e053-dadaa90a0b85COOLA Classic Body Sunscreen Guava Mango SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21839-450-01COOLA Classic Body Sunscreen Guava MangoSPF 50148 mL in 1 TUBELOTION1481
21839-450-02COOLA Classic Body Sunscreen Guava MangoSPF 501 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21839-450COOLA CLASSIC BODY SUNSCREEN GUAVA MANGO SPF 50 (AVOBENZONE,HOMOSALATE, OCTISALATE,OCTOCRYLENE) LOTION [GORDON LABORATORIES, INC.]1Legacy NDC, 2 package rows20191227_9aa24411-fdad-c256-e053-2a95a90a3649.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
21839-450-0121839045001148 mL in 1 TUBE148 mlHistorical
21839-450-02218390450021 in 1 CARTONHistorical