MediSpa Sunblock

Product NDC
52554-1001
11-digit product format
525541001
Labeler code
52554
Product ID
52554-1001_ad7e144f-288c-4513-86f1-c9d82bd80359
Type
HUMAN OTC DRUG
Nonproprietary name
zinc oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Universal Cosmetic Co., Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2010-08-04
Marketing end
0000-00-00
Substance
ZINC OXIDE; OCTINOXATE; ENZACAMENE; AVOBENZONE
Active strength
0 mL/mL; mL/mL; mL/mL; mL/mL
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
52554-1001-12019-10-21C16284748780-1956f9ecf-cf06-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-1001-1MediSpa Sunblocksunblock70 mL in 1 BOTTLE, WITH APPLICATORCREAM701

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-1001MEDISPA SUNBLOCK SUNBLOCK (ZINC OXIDE) CREAM [UNIVERSAL COSMETIC CO., LTD]1Legacy NDC, 1 package rows20100806_2eda1a2b-e024-449b-9553-839cdad9aab3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
52554-1001-15255410010170 mL in 1 BOTTLE, WITH APPLICATOR70 mlHistorical