Sunscreen and Amphibious

Product NDC
77714-004
Requested package NDC
77714-004-15
11-digit product format
777140004
Labeler code
77714
Product ID
77714-004_d621c6ca-f802-436c-e053-2995a90a4e34
Type
HUMAN OTC DRUG
Nonproprietary name
SPF 50
Dosage form
LOTION
Route
TOPICAL
Labeler
Bullfrog Brands, LLC
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-01-19
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30 mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage77714-00477714-004-15IInactivated by FDA2026-10-12

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage77714-00477714-004-15IInactivated by FDAexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage77714-00477714-004-15IInactivated by FDAexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

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
77714-004-152025-07-29C16284748780-13b156c62-25e6-fb37-e063-e6dba90a4e07Bull Frog SPF50 Amphibious lotion with Armor Tech

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77714-004-15Sunscreen and AmphibiousBull frog148 g in 1 BOTTLELOTION1482

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77714-004SUNSCREEN AND AMPHIBIOUS BULL FROG (SPF 50) LOTION [BULLFROG BRANDS, LLC]2Legacy NDC, 1 package rows20240126_d621c6ca-f801-436c-e053-2995a90a4e34.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
77714-004-1577714000415148 g in 1 BOTTLE (77714-004-15) 148 g2022-01-190000-00-00NoNoCurrent