Sunscreen and Amphibious

Product NDC: 77714-004
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	77714-004		I	Inactivated by FDA		2026-10-12
excluded package	package	77714-004	77714-004-15	I	Inactivated by FDA		2026-10-12

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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	77714-004-15	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	77714-004-15	`f5e01cc5f278…`	`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
NDC	Effective	Action	Document	Indexing SPL	Related label
77714-004-15	2025-07-29	C162847	48780-1	3b156c62-25e6-fb37-e063-e6dba90a4e07	Bull Frog SPF50 Amphibious lotion with Armor Tech

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77714-004-15	Sunscreen and AmphibiousBull frog	148 g in 1 BOTTLE	LOTION	148		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77714-004	SUNSCREEN AND AMPHIBIOUS BULL FROG (SPF 50) LOTION [BULLFROG BRANDS, LLC]	2	Legacy NDC, 1 package rows	20240126_d621c6ca-f801-436c-e053-2995a90a4e34.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
77714-004-15	77714000415	148 g in 1 BOTTLE (77714-004-15)	148 g	2022-01-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Bull Frog SPF50 Amphibious lotion with Armor Tech	Bullfrog Brands, LLC \| ARG Laboratories	2024-01-25	HUMAN OTC DRUG LABEL	2