COOLA Classic Face Sunscreen White Tea

Product NDC
21839-540
11-digit product format
218390540
Labeler code
21839
Product ID
21839-540_9aa4eb1c-7d6a-fa7a-e053-2995a90a2f01
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
2019-02-12
Marketing end
0000-00-00
Substance
OCTISALATE; OCTOCRYLENE; HOMOSALATE; AVOBENZONE
Active strength
20 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
21839-540-022021-01-29C16284748780-1ba0f9c33-35fd-a910-e053-dadaa90a0b85COOLA Classic Face Sunscreen White Tea SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21839-540-01COOLA Classic Face Sunscreen White TeaSPF 50148 mL in 1 TUBELOTION1481
21839-540-02COOLA Classic Face Sunscreen White TeaSPF 501 in 1 CARTONLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21839-540COOLA CLASSIC FACE SUNSCREEN WHITE TEA SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [GORDON LABORATORIES, INC.]1Legacy NDC, 2 package rows20191228_9aa4eb29-3490-7b7c-e053-2a95a90a20fc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
21839-540-0121839054001148 mL in 1 TUBE148 mlHistorical
21839-540-02218390540021 in 1 CARTONHistorical