No7 Lift and Luminate Triple Action Day Cream SPF 30

Product NDC: 11489-182
11-digit product format: 114890182
Labeler code: 11489
Product ID: 11489-182_4f5b963a-6dad-3ee8-e063-6294a90a4481
Type: HUMAN OTC DRUG
Nonproprietary name: Avobenzone, Octisalate, Octocrylene
Dosage form: CREAM
Route: TOPICAL
Labeler: BCM Ltd
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-08-17
Substance: AVOBENZONE; OCTOCRYLENE; OCTISALATE
Active strength: 1.5; 3.75; 2.5 g/50g; g/50g; g/50g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11489-182-01	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11489-182-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11489-182-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11489-182-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11489-182-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11489-182-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11489-182-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11489-182-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11489-182-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: No7 Lift and Luminate Triple Action Day Cream SPF 30
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
AVOBENZONE	1.5 g/50g
OCTOCRYLENE	3.75 g/50g
OCTISALATE	2.5 g/50g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G63QQF2NOX	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
4X49Y0596W	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
f7d5aa8a-9f4a-426b-ac9d-9690cf0103e0	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11489-182-01	2025-01-30	C162847	48780-1	2cef2736-b15a-d83d-e063-dadaa90ab31f	No7 Lift and Luminate Triple Action Day Cream Sunscreen Broad Spectrum SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11489-182-01	No7 Lift and Luminate Triple Action Day Cream SPF 30	1 in 1 CARTON	CREAM	1		2
11489-182-01	No7 Lift and Luminate Triple Action Day Cream SPF 30	50 g in 1 JAR	CREAM	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11489-182	NO7 LIFT AND LUMINATE TRIPLE ACTION DAY CREAM SPF 30 (AVOBENZONE, OCTISALATE, OCTOCRYLENE) CREAM [BCM LTD]	1	Current NDC, Legacy NDC, 2 package rows	20210819_f7d5aa8a-9f4a-426b-ac9d-9690cf0103e0.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 145 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Perfecting Blendrops Broad Spectrum SPF 40	HOMOSALATE, OCTISALATE, ZINC OXIDE	Wasatch Product Development, LLC	12512cac-652e-b138-e063-6394a90ad1f2	2025-12-09	Warnings	Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ASHLEY SAMAI	38f457fa-0e95-7298-e063-6394a90adda8	2025-12-09		Exact identifier application number: M020
Non-Tinted Mineral Sunscreen	ZINC OXIDE	OLGA KLIMOV INC	387b41a4-057f-88af-e063-6394a90adbbe	2025-12-09		Exact identifier application number: M020
Tinted Replenishing Daily Protection	ZINC OXIDE	OLGA KLIMOV INC	387b8ae6-c48b-905c-e063-6394a90a31fb	2025-12-09		Exact identifier application number: M020
Tinted Primer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CECILIA EDWARDS	36ea709b-3536-5052-e063-6394a90a48f9	2025-12-09		Exact identifier application number: M020
Age Defying Mineral Protection	TITANIUM DIOXIDE, ZINC OXIDE	MARK SCHWARTZ CLINICAL SKINCARE, INC.	3b028159-f240-2cf2-e063-6294a90a32b5	2025-12-09	Warnings	Exact identifier application number: M020
Ultimate Mineral Protection	ZINC OXIDE	MARK SCHWARTZ CLINICAL SKINCARE, INC.	3b02bf69-b648-56e1-e063-6294a90aeef3	2025-12-09	Warnings	Exact identifier application number: M020
G.M. Collin FPS-SPF 45 UVA-UVB TINTED SUNSCREEN	ZINC OXIDE, TITANIUM DIOXIDE	LABORATOIRES DERMO-COSMETIK INC.	01dcfd14-7a1d-98fa-e063-6294a90a0336	2025-12-09	Warnings	Exact identifier application number: M020
Tinted Primer Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CECILIA EDWARDS	3aff2074-1514-b5c5-e063-6394a90a7572	2025-12-09		Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER	3729d270-64ac-4d2e-e063-6294a90aeb2c	2025-12-09		Exact identifier application number: M020
Non Tinted Replenishing Daily Protection	ZINC OXIDE	LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER	372a41f6-40f6-4971-e063-6394a90a83e0	2025-12-09		Exact identifier application number: M020
Stay Shady Non-Tinted Mineral Sunscreen	ZINC OXIDE	AMOIE ALAYVILLA	3b277237-3a2e-1fb0-e063-6294a90adf20	2025-12-09	Warnings	Exact identifier application number: M020
Stay Shady Non-Tinted Mineral Sunscreen	ZINC OXIDE	AMOIE ALAYVILLA	3b27225f-4589-d915-e063-6294a90a7225	2025-12-09	Warnings	Exact identifier application number: M020
Replenishing Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Beauty Journey Studio LLC	3738a0c3-5c07-e49b-e063-6394a90a38e9	2025-12-09		Exact identifier application number: M020
Replenishing Non Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Beauty Journey Studio LLC	37385fc6-1cde-8aa6-e063-6294a90a6017	2025-12-09		Exact identifier application number: M020
Replenishing Tinted Sunscreen	ZINC OXIDE	Beauty Journey Studio LLC	3738e5e0-f6d9-0568-e063-6294a90a67b6	2025-12-09		Exact identifier application number: M020
JAYSUING Matte Sun Stick	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456b44da-02f3-93a0-e063-6294a90a8d06	2025-12-08	Warnings	Exact identifier application number: M020
JAYSUING Matte Sun Stick	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456c2974-d499-7841-e063-6294a90a98eb	2025-12-08	Warnings	Exact identifier application number: M020
JAYSUING Ginseng Moist Sun Serum	TITANIUM DIOXIDE	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	456cfa70-f524-f5cb-e063-6394a90ae7dc	2025-12-08	Warnings	Exact identifier application number: M020
Face and Body Sunscreen	NON-NANO ZINC OXIDE 25%	Guangzhou Shengyanghui Industrial Trading Co., Ltd	3ee96538-06e8-75b1-e063-6394a90a5285	2025-12-08	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
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
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
11489-182-01	11489018201	1 JAR in 1 CARTON (11489-182-01) / 50 g in 1 JAR	1 jar	2021-08-17	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
No7 Lift and Luminate Triple Action Day Cream Sunscreen Broad Spectrum SPF 30	BCM Ltd \| The Boots Company PLC	2026-01-01	HUMAN OTC DRUG LABEL	2