Sheer Fluid Sun Shield

Product NDC
72704-108
Requested package NDC
72704-108-01
11-digit product format
727040108
Labeler code
72704
Product ID
72704-108_37a86e13-e7e7-489b-a1df-021a18522595
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate and Zinc Oxide
Dosage form
LIQUID
Route
TOPICAL
Labeler
Lancer Skincare LLC.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-11-01
Marketing end
0000-00-00
Substance
OCTINOXATE; ZINC OXIDE
Active strength
8 g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72704-10872704-108-01IInactivated by FDA2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72704-108-012025-01-30C16284748780-12cef2736-7188-d83d-e063-dadaa90ab31fSheer Fluid Sun Shield Broad Spectrum SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72704-108-01Sheer Fluid Sun Shield Broad Spectrum SPF 301 in 1 CARTONLIQUID12
72704-108-01Sheer Fluid Sun Shield Broad Spectrum SPF 3060 mL in 1 BOTTLELIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72704-108SHEER FLUID SUN SHIELD BROAD SPECTRUM SPF 30 (OCTINOXATE AND ZINC OXIDE) LIQUID [LANCER SKINCARE LLC.]2Legacy NDC, 2 package rows20230126_625037c2-f5f8-4391-baed-7204ca287f35.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72704-108-01727040108011 BOTTLE in 1 CARTON (72704-108-01) > 60 mL in 1 BOTTLE1 bottle2016-11-010000-00-00NoNoCurrent