Sunscreen Wipe

Product NDC
52648-6175
11-digit product format
526486175
Labeler code
52648
Product ID
52648-6175_556865f0-7dda-46b4-9948-d987b95f740f
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE
Dosage form
CLOTH
Route
TOPICAL
Labeler
KGP Products, Inc. (dba PREMIER)
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-09-28
Marketing end
0000-00-00
Substance
HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength
20 g/856mL; g/856mL; g/856mL; g/856mL
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
52648-6175-12019-10-21C16284748780-1956f9ecf-d137-621f-e053-dbdaa90a74adc649a9be-5e7a-4436-aea1-017e36b07d08

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52648-6175-1Sunscreen WipeKGP9 mL in 1 PACKETCLOTH92

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52648-6175SUNSCREEN WIPE KGP (HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE ) CLOTH [KGP PRODUCTS, INC. (DBA PREMIER)]2Legacy NDC, 1 package rows20101001_c649a9be-5e7a-4436-aea1-017e36b07d08.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
52648-6175-1526486175019 mL in 1 PACKET9 mlHistorical