FDA.reportPublic FDA data

SPF 30 Sport Sunscreen

Product NDC
55165-0204
11-digit product format
551650204
Labeler code
55165
Product ID
55165-0204_e1552d9d-74cc-472c-91d5-95f8438bba06
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Juice Beauty
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-06-03
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
20 g/100mL
NDC exclude flag
No
Listing certified through
2024-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct55165-0204IInactivated by FDA2026-10-12
excluded packagepackage55165-020455165-0204-1IInactivated by FDA2026-10-12

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55165-0204-1SPF 30 Sport Sunscreen90 mL in 1 TUBELOTION903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55165-0204SPF 30 SPORT SUNSCREEN (ZINC OXIDE) LOTION [JUICE BEAUTY]3Legacy NDC, 1 package rows20241225_dc0fc276-32b3-407d-8de2-b814de2e222b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55165-0204-15516502040190 mL in 1 TUBE (55165-0204-1) 90 ml2014-06-030000-00-00NoNoCurrent