SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE plus 1ST SIGNS OF AGE MULTI-CORRECTING

Product NDC: 49527-075
11-digit product format: 495270075
Labeler code: 49527
Product ID: 49527-075_f0d8b591-7ead-7fc7-e053-2a95a90a04e6
Type: HUMAN OTC DRUG
Nonproprietary name: AVOBENZONE and OCTISALATE
Dosage form: CREAM
Route: TOPICAL
Labeler: CLINIQUE LABORATORIES LLC
Application: M020
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-11-21
Marketing end: 0000-00-00
Substance: AVOBENZONE; OCTISALATE
Active strength: 0 g/mL; g/mL
NDC exclude flag: No
Listing certified through: 2024-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	49527-075		I	Inactivated by FDA	2026-11-13
excluded package	package	49527-075	49527-075-01	I	Inactivated by FDA	2026-11-13
excluded package	package	49527-075	49527-075-02	D	Discontinued by firm	2026-11-13

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.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7dea7767-9f52-b60a-5435-33cb9cc28bae	Product name	4	20250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4	Product name	7	20250116
0ca83774-3f79-b837-5d6f-c210102f3bc8	Product name	6	20250114
41b814f3-0166-1c53-c9ef-a0794c7daf9d	Product name	3	20221110
a590be26-846c-8659-a5a1-fb25907965dc	Product name	2	20221110
2dc76302-91c0-4c35-ad78-99adfb049c4b	Product name	1	20200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2b	Product name	2	20180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
332e86c3-7875-ca6e-f934-2206d2b31996	Product name	1	20140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21	Product name	1	20140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508
d223c173-c39b-d764-47d4-d671d3088815	Product name	1	20140508
e01133ad-4dcd-c7f3-454b-2ff569ee160a	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49527-075-01	2022-08-15	C162847	48780-1	e4f33bdf-9e69-d8a0-e053-dadaa90a6e4e	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE + 1ST SIGNS OF AGE MULTI-CORRECTING CREAM
49527-075-01	2022-07-29	C162847	48780-1	e4f33bdf-9e69-d8a0-e053-dadaa90a6e4e	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE + 1ST SIGNS OF AGE MULTI-CORRECTING CREAM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
49527-075-01	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE plus 1ST SIGNS OF AGE MULTI-CORRECTING	1 in 1 CARTON	CREAM	1	9
49527-075-01	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE plus 1ST SIGNS OF AGE MULTI-CORRECTING	50 mL in 1 JAR	CREAM	50	9
49527-075-02	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE plus 1ST SIGNS OF AGE MULTI-CORRECTING	7 mL in 1 TUBE	CREAM	7	9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49527-075	SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE PLUS 1ST SIGNS OF AGE MULTI-CORRECTING (AVOBENZONE AND OCTISALATE) CREAM [CLINIQUE LABORATORIES LLC]	9	Legacy NDC, 3 package rows	20241226_53c03415-5a4c-492a-b632-56699c042bec.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 290 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Clarity Rx Pucker Power lip plumper SPF 30	HOMOSALATE, OCTINOXATE, OCTISALATE, AVOBENZONE	Topiderm, Inc.	92504982-fe0e-404d-b7cf-f6b340b89802	2024-07-31	Warnings	Exact identifier application number: M020
Essential Sheer SPF 50	ZINC OXIDE TITANIUM DIOXIDE	Topiderm, Inc.	2132dc18-85ee-4449-86d2-d9f698f286c6	2024-07-31	Warnings	Exact identifier application number: M020
Proceuticals Private Label by TiZO tinted foaming mineral sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, Ltd	1e78109f-4d2e-2705-e063-6294a90a5ad3	2024-07-30	Warnings	Exact identifier application number: M020
Replenix Sheer SPF 50	ZINC OXIDE TITANIUM DIOXIDE	Topiderm, Inc.	37d1f454-3bc9-4ce5-863c-0d4f6fa18fb4	2024-07-29	Warnings	Exact identifier application number: M020
Dr Pawpaw MultiPurpose Lip Balm with natural PawPaw and SPF 30	AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE, OCTISALATE	Dr Pawpaw Limited	f2628e3e-9eb0-49cb-91a6-d15c48cb8a19	2024-07-25	Warnings	Exact identifier application number: M020
Thinksport Daily Face SPF 50	ZINC OXIDE	thinkOperations,LLC	b2422785-bd35-4248-a68f-fb4b1492a4cd	2024-07-24	Warnings	Exact identifier application number: M020
Thinkbaby Clear Zinc SPF 30	ZINC OXIDE	thinkOperations,LLC	7cd9c971-5556-42dc-af7b-3a88221b8c94	2024-07-24	Warnings	Exact identifier application number: M020
ISNTREE ONION NEWPAIR SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	ISNTREE Inc.	0f072099-d57d-4dc4-e063-6394a90ab438	2024-07-23	Warnings	Exact identifier application number: M020
ISNTREE ONION NEWPAIR SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	ISNTREE Inc.	14b11b42-d1fe-572f-e063-6394a90a9eec	2024-07-23	Warnings	Exact identifier application number: M020
Proceuticals Private Label by TiZO tinted mineral sunscreen 20% zinc oxide	ZINC OXIDE	Fallien Cosmeceuticals, Ltd	1dda8259-4121-3c76-e063-6394a90af189	2024-07-22	Warnings	Exact identifier application number: M020
Eco Lips PlantPod Sunscreen Lip Balm Sport SPF 30	AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE	Eco Lips. Inc.	e64c8644-7af4-7b7f-e053-2995a90af711	2024-07-22	Warnings	Exact identifier application number: M020
Thinksport SPF 30	ZINC OXIDE	thinkOperations,LLC	2cecda56-4860-4d35-abc2-2bb9bdf35eae	2024-07-19	Warnings	Exact identifier application number: M020
CVS Health SPORT SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	CVS PHARMACY	f0e8c724-b377-5dc0-e053-2995a90a0d54	2024-07-18	Warnings	Exact identifier application number: M020
EQUATE Sunscreen SPORT Broad Spectrum SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	WAL-MART STORES INC	4d819fd3-de12-4394-82f4-a48faf0b7092	2024-07-18	Warnings	Exact identifier application number: M020
Big Lots Soundbody SPF 30 Ultra Sport Sunscreen	AVOBENZONE HOMOSALATE OCTOCRYLENE	BIG LOTS STORES, INC.	f0e82a9f-17ac-b1c5-e053-2995a90ae07a	2024-07-18	Warnings	Exact identifier application number: M020
Equaline SPORT Sunscreen SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	United Natural Foods, Inc. dba UNFI	f0e8dfd4-a77c-6384-e053-2a95a90a1e4a	2024-07-18	Warnings	Exact identifier application number: M020
TopCare Everyday SPORT Sun Broad Spectrum SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	TOPCO ASSOCIATES LLC	f0e93aa8-1b09-1312-e053-2a95a90a7934	2024-07-18	Warnings	Exact identifier application number: M020
Safeway Signature Sport Sunscreen SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	Safeway, Inc.	f557a3e2-e415-1b65-e053-2995a90a987a	2024-07-18	Warnings	Exact identifier application number: M020
Target Up and Up Sunscreen Sport Broad Spectrum SPF 30	AVOBENZONE HOMOSALATE OCTOCRYLENE	TARGET CORPORATION	bad60bc1-cf78-7a33-e053-2995a90afdc3	2024-07-18	Warnings	Exact identifier application number: M020
Scar Gel SPF 35	ZINC OXIDE	derma e	8cd263aa-a54b-4c55-b3e2-6f6763987d4a	2024-07-17	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49527-075-01	49527007501	1 JAR in 1 CARTON (49527-075-01) > 50 mL in 1 JAR	1 jar	2019-11-21	0000-00-00	No	No	Current
49527-075-02	49527007502	7 mL in 1 TUBE (49527-075-02)	7 ml	2019-11-21	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SUPERDEFENSE BROAD SPECTRUM SPF 25 FATIGUE + 1ST SIGNS OF AGE MULTI-CORRECTING CREAM	CLINIQUE LABORATORIES LLC \| Estee Lauder Companies Inc. \| PALC \| The Estee Lauder Inc \| NORTHTEC LLC	2024-12-25	HUMAN OTC DRUG LABEL	9