Home NDC 60934-011-00 HydroPeptide Solar Defense Hand Guard
Product NDC 60934-011
Requested package NDC 60934-011-00
11-digit product format 609340011
Labeler code 60934
Product ID 60934-011_ce9d9647-0817-1467-e053-2995a90aede2
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE, ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler HydroPeptide LLC
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2021-01-01
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 13 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60934-011-00 HydroPeptide S.P.F. Sun Protection Friends 1 in 1 CARTON CREAM 12.5 mg in 1mL 3 60934-011-00 HydroPeptide S.P.F. Sun Protection Friends 75 mL in 1 TUBE CREAM 75 mL 12.5 mg in 1mL 3 60934-011-00 HydroPeptide Solar Defense Hand Guard 1 in 1 CARTON CREAM 1 1 60934-011-00 HydroPeptide Solar Defense Hand Guard 75 mL in 1 TUBE CREAM 75 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60934-011 HYDROPEPTIDE S.P.F. SUN PROTECTION FRIENDS (TITANIUM DIOXIDE, ZINC OXIDE) KIT [HYDROPEPTIDE LLC] 3 Legacy NDC 20250130_f3669a1e-8b75-4e94-a3f0-71dcbc3fa914.zip 60934-011 HYDROPEPTIDE SOLAR DEFENSE HAND GUARD (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HYDROPEPTIDE LLC] 1 Legacy NDC, 2 package rows 20211020_1002ce35-e8ac-470f-8818-328a8068ccb1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60934-011-00 60934001100 1 TUBE in 1 CARTON (60934-011-00) > 75 mL in 1 TUBE 1 tube 2021-01-01 0000-00-00 No No Current