LOreal Paris Infallible ProGlow Broad Spectrum SPF 15 Sunscreen

Product NDC: 49967-043
11-digit product format: 499670043
Labeler code: 49967
Product ID: 49967-043_6a9b680d-ea91-44fd-94fd-bee18621aca2
Type: HUMAN OTC DRUG
Nonproprietary name: Octinoxate
Dosage form: LIQUID
Route: TOPICAL
Labeler: L'Oreal USA Products Inc
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-02-26
Substance: OCTINOXATE
Active strength: 32 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	49967-043	49967-043-01	D	Discontinued by firm		2026-10-28

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: LOreal Paris Infallible ProGlow Broad Spectrum SPF 15 Sunscreen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	32 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
82a6fbba-f0d4-475f-9ba7-615118eed70d	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49967-043-01	LOreal Paris Infallible ProGlow Broad Spectrum SPF 15 Sunscreen	30 mL in 1 BOTTLE	LIQUID	30		3
49967-043-02	LOreal Paris Infallible ProGlow Broad Spectrum SPF 15 Sunscreen	30 mL in 1 TUBE	LIQUID	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49967-043	LOREAL PARIS INFALLIBLE PROGLOW BROAD SPECTRUM SPF 15 SUNSCREEN (OCTINOXATE) LIQUID [L'OREAL USA PRODUCTS INC]	3	Current NDC, Legacy NDC, 2 package rows	20231230_82a6fbba-f0d4-475f-9ba7-615118eed70d.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 194 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sun Bum Broad Spectrum SPF 30 5 OZ	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3cad0757-3155-c716-e063-6294a90ad7a9	2025-08-18	Warnings	Exact identifier application number: M020
Cica Redness Solution Sunscreen	ZINC OXIDE	Meebak Beauty, Inc	15eea1eb-9468-4611-915d-e43112c4a4f5	2025-08-18	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE/OCTOCRYLENE	Edgewell Personal Care Brands LLC	3c936ed0-ab7a-ccec-e063-6294a90afd93	2025-08-17	Warnings	Exact identifier application number: M020
Banana Boat	AVOBENZONE OCTOCRYLENE OXYBENZONE	Edgewell Personal Care Brands LLC	0f772b91-e67b-46cf-e054-00144ff8d46c	2025-08-17	Warnings	Exact identifier application number: M020
BANANA BOAT	AVOBENZONE, OCTOCRYLENE, OXYBENZONE	EdgewellPersonal Care Brands LLC	353353b9-54f8-4300-9632-7615de394076	2025-08-17	Warnings	Exact identifier application number: M020
BANANA BOAT	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	0c6aeadb-f61d-29e3-e063-6294a90a7473	2025-08-17	Warnings	Exact identifier application number: M020
MOISTURE SURGE SPF	AVOBENZONE,HOMOSALATE,OCTINOXATE,OCTISALATE	CLINIQUE LABORATORIES LLC	ec921e21-db68-db77-e053-2a95a90a5781	2025-08-15	Warnings	Exact identifier application number: M020
Olay Invisible Sunscreen Facial Primer plus Sunscreen Broad Spectrum SPF 35	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	3c69f096-1575-309b-e063-6394a90a7229	2025-08-15	Warnings	Exact identifier application number: M020
MOISTURE SURGE CC BROAD SPECTRUM SPF 30 HYDRATING COLOUR CORRECTOR	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AND ZINC OXIDE	CLINIQUE LABORATORIES LLC	ea4d564f-ac64-abac-e053-2a95a90a8abb	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum Tinted Sunscreen Lip Balm Broad Spectrum SPF 15 - Sunset Cove Carded	HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE	Sun Bum, LLC	3ac67c26-d56e-32a9-e063-6294a90a1048	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum Signature High Performance Mineral Sunscreen Broad Spectrum SPF 50	ZINC OXIDE	Sun Bum, LLC	3aa13423-045a-7227-e063-6294a90ae49b	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum Daily Sunscreen Mist Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	3a796a0b-8021-9a9f-e063-6294a90a6eb2	2025-08-15	Warnings	Exact identifier application number: M020
SOLARA SUNCARE - DAY DREAMER SPF 30	ZINC OXIDE	SOLARA SUNCARE, INC.	3c6c9266-a7ff-19f4-e063-6294a90a6096	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum Mineral 30 Sheer Sunscreen Face	ZINC OXIDE	Sun Bum, LLC	3b00c2d6-a55d-0a56-e063-6294a90ac4b8	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum Mineral 30 Sunscreen 3 OZ	ZINC OXIDE	Sun Bum, LLC	3b014bd6-ba40-9003-e063-6394a90ab451	2025-08-15	Warnings	Exact identifier application number: M020
Ocean Potion Suncare Mineral 30 Zinc Oxide Sunscreen	ZINC OXIDE	GNL BRANDS INTERNATIONAL, LLC	3c6e7e62-4313-cbce-e063-6394a90ac382	2025-08-15	Warnings	Exact identifier application number: M020
Ocean Potion Face with Clear Zinc Oxide Broad Spectrum SPF 50 Sunscreen	OCTOCRYLENE, ZINC OXIDE	GNL BRANDS INTERNATIONAL, LLC	3c6f3e0b-2dff-6dc3-e063-6394a90abb0e	2025-08-15	Warnings	Exact identifier application number: M020
EltaMD UV Daily Hydration	OCTISALATE, ZINC OXIDE SUNSCREEN	CP Skin Health Group, Inc.	bfdb266b-9920-4225-84c7-bcbad81fd1c7	2025-08-15	Warnings	Exact identifier application number: M020
Sun Bum 70 Premium Moisturizing Sunscreen 8 OZ	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	39fb5e66-5172-3b83-e063-6394a90aab2d	2025-08-14	Warnings	Exact identifier application number: M020
Sun Bum Face Cream 50 Premium Sunscreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE	Sun Bum, LLC	3c57fcf7-7816-8197-e063-6394a90af80a	2025-08-14	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49967-043-01	49967004301	30 mL in 1 BOTTLE (49967-043-01)	30 ml	2016-02-26	0000-00-00	No	No	Current
49967-043-02	49967004302	30 mL in 1 TUBE (49967-043-02)	30 ml	2016-02-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	L'Oreal USA Products Inc \| L'Oreal USA Products, Inc.	2023-12-29	HUMAN OTC DRUG LABEL	3