LA Bodies Eclipse Sunscreen SPF 50

Product NDC: 20146-4008
11-digit product format: 201464008
Labeler code: 20146
Product ID: 20146-4008_d11589cb-2061-4c53-8d81-76ebf8a94a96
Type: HUMAN OTC DRUG
Nonproprietary name: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Dosage form: LOTION
Route: TOPICAL
Labeler: SAMSON PHARMACEUTICAL
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-01-01
Substance: AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength: 30; 150; 50; 24; 60 mg/g; mg/g; mg/g; mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: LA Bodies Eclipse Sunscreen SPF 50
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
AVOBENZONE	30 mg/g
HOMOSALATE	150 mg/g
OCTISALATE	50 mg/g
OCTOCRYLENE	24 mg/g
OXYBENZONE	60 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G63QQF2NOX	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
95OOS7VE0Y	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
ce3a5ddc-9d4d-4d63-879c-fc4aef9a0a0a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
20146-4008-1	2022-01-31	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-2	2022-01-31	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-1	2022-01-28	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-2	2022-01-28	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-1	2020-02-12	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-2	2020-02-12	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-1	2020-01-31	LA Bodies ® Eclipse Sunscreen Lotion SPF 50
20146-4008-2	2020-01-31	LA Bodies ® Eclipse Sunscreen Lotion SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
20146-4008-1	LA Bodies Eclipse Sunscreen SPF 50	28 g in 1 TUBE	LOTION	28		4
20146-4008-2	LA Bodies Eclipse Sunscreen SPF 50	85 g in 1 TUBE	LOTION	85		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Avobenzone	ACTIVE INGREDIENT	G63QQF2NOX	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Homosalate	ACTIVE INGREDIENT	V06SV4M95S	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Octisalate	ACTIVE INGREDIENT	4X49Y0596W	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Octocrylene	ACTIVE INGREDIENT	5A68WGF6WM	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Oxybenzone	ACTIVE INGREDIENT	95OOS7VE0Y	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Avobenzone	ACTIVE MOIETY	G63QQF2NOX	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Homosalate	ACTIVE MOIETY	V06SV4M95S	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Octisalate	ACTIVE MOIETY	4X49Y0596W	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Octocrylene	ACTIVE MOIETY	5A68WGF6WM	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
Oxybenzone	ACTIVE MOIETY	95OOS7VE0Y	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
cetyl alcohol	INACTIVE INGREDIENT	936JST6JCN	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
glyceryl monostearate	INACTIVE INGREDIENT	230OU9XXE4	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
PEG-100 stearate	INACTIVE INGREDIENT	YD01N1999R	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
stearyl alcohol	INACTIVE INGREDIENT	2KR89I4H1Y	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1
water	INACTIVE INGREDIENT	059QF0KO0R	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
20146-4008	LA BODIES ECLIPSE SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE) LOTION [SAMSON PHARMACEUTICAL]	4	Current NDC, Legacy NDC, 2 package rows	20240120_ce3a5ddc-9d4d-4d63-879c-fc4aef9a0a0a.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 114 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Zinc 20 mineral sunscreen face Plus body	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	36985373-22dd-2232-e063-6394a90a76fb	2025-12-16		Exact identifier application number: M020
Matte Defense Mineral Sunscreen non tinted	TITANIUM DIOXIDE, ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698090a-1639-00f9-e063-6394a90a7dd1	2025-12-16		Exact identifier application number: M020
Daily Replenish mineral sunscreen	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698d309-b9bf-e197-e063-6294a90af5a1	2025-12-16		Exact identifier application number: M020
Zinc 20 mineral sunscreen face Plus body	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698f29e-5d80-94af-e063-6394a90a0489	2025-12-16		Exact identifier application number: M020
Tinted Mineral Primer SPF 40	TITANIUM DIOXIDE, ZINC OXIDE	JOSEPHINA RAMIREZ	365cf2be-8862-3622-e063-6394a90ac4e3	2025-12-16		Exact identifier application number: M020
SANCTUARY Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CHAMPAGNE APOTHECARY LLC	365ca99c-c878-1f4b-e063-6394a90a1f53	2025-12-16		Exact identifier application number: M020
Tinted Mineral Defense SPF 40	ZINC OXIDE	JOSEPHINA RAMIREZ	365d299a-5886-5597-e063-6394a90a336c	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	MILL VALLEY DERMATOLOGY, INC.	3b171a89-c757-47a1-e063-6294a90a7a64	2025-12-16	Warnings	Exact identifier application number: M020
Tinted BB Cream	ZINC OXIDE	Eco Esthetics LLC	38f3e618-59e1-4504-e063-6394a90afa55	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	ZINC OXIDE	MADRE TIERRA, INC.	3f697463-d3db-7b73-e063-6394a90ac222	2025-12-16	Warnings	Exact identifier application number: M020
Non-Tinted Replenishing Daily Protection	ZINC OXIDE	MADRE TIERRA, INC.	3f69d6f3-454b-e60a-e063-6394a90a8781	2025-12-16	Warnings	Exact identifier application number: M020
Mineral Sunscreen	ZINC OXIDE	ISIS GONZALEZ	3f68b2ea-be23-100d-e063-6294a90a8b37	2025-12-16	Warnings	Exact identifier application number: M020
Mineral Sunscreen	ZINC OXIDE	ISIS GONZALEZ	3f682b78-e1c9-e174-e063-6294a90a17ed	2025-12-16	Warnings	Exact identifier application number: M020
Silk Screen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Skin Science Institute Inc	36c3793a-ccb5-1e5f-e063-6294a90ad44f	2025-12-16		Exact identifier application number: M020
Silk Screen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Skin Science Institute Inc	36c3a721-6be1-3f7f-e063-6394a90a522f	2025-12-16		Exact identifier application number: M020
True Tone Tinted	TITANIUM DIOXIDE, ZINC OXIDE	That Face PLLC	36c2bb0e-479d-89cd-e063-6294a90aa3d4	2025-12-16		Exact identifier application number: M020
True Tone Non Tinted	ZINC OXIDE	That Face PLLC	36c2f263-67cf-e8cf-e063-6394a90ad81f	2025-12-16		Exact identifier application number: M020
Tinted Daily Protection Sunscreen	ZINC OXIDE	Kemmi Lee Skin Science	37ef5a05-54d2-a8e4-e063-6394a90a8e48	2025-12-16		Exact identifier application number: M020
Aquaphor Lip Repair Stick and Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE,	Beiersdorf Inc	d469bddf-90d4-7b1c-e053-2a95a90a1ed9	2025-12-16	Warnings	Exact identifier application number: M020
Eucerin Daily Protection Face	ENSULIZOLE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE	Beiersdorf Inc	76403f03-aee9-4c0b-b331-f79b6953118c	2025-12-16	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
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
20146-4008-1	20146400801	28 g in 1 TUBE (20146-4008-1)	28 g	2015-01-01	0000-00-00	No	No	Current
20146-4008-2	20146400802	85 g in 1 TUBE (20146-4008-2)	85 g	2015-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
LA Bodies ® Eclipse Sunscreen Lotion SPF 50	SAMSON PHARMACEUTICAL	2024-01-18	HUMAN OTC DRUG LABEL	4