Sunplus SPF50 Face Body Sunscreen

Product NDC: 65112-304
11-digit product format: 651120304
Labeler code: 65112
Product ID: 65112-304_4a08871f-25e4-215d-e063-6394a90ab8a8
Type: HUMAN OTC DRUG
Nonproprietary name: Sunscreen
Dosage form: LOTION
Route: TOPICAL
Labeler: I.Shay Cosmetics
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2004-06-01
Substance: OCTOCRYLENE; OCTISALATE; AVOBENZONE; HOMOSALATE
Active strength: .06; .05; .02; .15 g/118mL; g/118mL; g/118mL; g/118mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Sunplus SPF50 Face Body Sunscreen
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTOCRYLENE	.06 g/118mL
OCTISALATE	.05 g/118mL
AVOBENZONE	.02 g/118mL
HOMOSALATE	.15 g/118mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5A68WGF6WM	Internal UNII lookup
4X49Y0596W	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
V06SV4M95S	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
26d55baf-66dc-b1b8-e063-6394a90a670d	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
65112-304-01	2026-01-29	C162847	48780-1	49896155-b02f-586f-e063-e6dba90add90	Sunplus SFP50 Face Body Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65112-304-01	Sunplus SPF50 Face Body Sunscreen	118 mL in 1 TUBE	LOTION	118		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65112-304	SUNPLUS SPF50 FACE BODY SUNSCREEN (SUNSCREEN) LOTION [I.SHAY COSMETICS]	1	Current NDC, 1 package rows	20241115_26d55baf-66dc-b1b8-e063-6394a90a670d.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 251 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Oars and Alps SPF 50 Mineral	ZINC OXIDE	Oars and Alps LLC	f395bc39-daa5-53b8-e053-2995a90a5f48	2024-12-20	Warnings	Exact identifier application number: M020
Babyganics Kids Sheer Blend SPF50 Mineral Sunscreen	ZINC OXIDE	KAS Direct LLC dba BabyGanics	8a143645-3b52-4797-9b26-dc9dd63be38f	2024-12-20	Warnings	Exact identifier application number: M020
Nuria Defend Matte Finish Daily Moisturizer Mineral Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	Small World Brands	b1df4c81-333b-450d-963e-6670ab9bbda9	2024-12-20	Warnings	Exact identifier application number: M020
foundcealer multi-tasking foundation Broad Spectrum SPF 20 Sunscreen 8B porcelain beige	TITANIUM DIOXIDE AND ZINC OXIDE	Tarte, Inc.	062fa0d9-f384-48af-8269-42de3a788db1	2024-12-20	Warnings	Exact identifier application number: M020
Stokoderm Sunscreen PURE	AVOBENZONE, OCTOCRYLENE, OCTISALATE, AND HOMOSALATE	SC Johnson Professional USA, Inc.	3ddf81e6-de78-4f2f-814b-c75eadcddb39	2024-12-20	Warnings	Exact identifier application number: M020
BabyGanics Sunscreen 30 SPF	ZINC OXIDE, OCTINOXATE, AND OCTISALATE	KAS Direct LLC dba BabyGanics	391a4ec3-b65b-4dbe-bc8f-cb67514c8ef1	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 PORCELAIN	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299ac9a5-f609-d804-e063-6394a90abd05	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 IVORY	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299ad424-16a8-66b1-e063-6394a90a0753	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 NUDE	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299afef9-758f-74e1-e063-6294a90a8072	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 NATURAL BEIGE	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299b3276-7973-d33f-e063-6294a90a6ce1	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CLASSIC TAN	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299afe24-d496-5745-e063-6394a90aa1b3	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 WARM BEIGE	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299b1f9a-34fd-cb50-e063-6394a90af925	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SOFT SAND	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299b3236-3f3d-c9e8-e063-6394a90a7443	2024-12-19	Warnings	Exact identifier application number: M020
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 TAWNY	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	299b416d-ce02-3462-e063-6294a90a38f0	2024-12-19	Warnings	Exact identifier application number: M020
Puttisu	TITANIUM DIOXIDE, ZINC OXIDE	Jellycup, Inc.	a032331a-6724-d2cd-e053-2995a90ac15a	2024-12-19	Warnings	Exact identifier application number: M020
Dr. C. Tuna Resurface Essential Day Cream SPF 30	HOMOSALATE, OCTINOXATE, OCTOCRYLENE, AVOBENZONE	Farmasi US LLC	de493e30-d135-9def-e053-2995a90ae49a	2024-12-19	Warnings	Exact identifier application number: M020
toty Ilumina CC Cream 1N	TITANIUM DIOXIDE, ZINC OXIDE	Chipican LLC	e4efe14e-7d46-78c0-e053-2995a90a2364	2024-12-19	Warnings	Exact identifier application number: M020
Aruba Sun SPF 50 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	d8b28ce6-e938-c6e3-e053-2a95a90acc29	2024-12-19	Warnings	Exact identifier application number: M020
DCH Pain Relief Roll-On	LIDOCAINE HCL 4%	Derma Care Research Labs, LLC	fda35d37-f36e-efc8-e053-6294a90a2bb8	2024-12-19	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50 Kids	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	d53ff8f5-0b06-1e8b-e053-2a95a90ab924	2024-12-19	Warnings	Exact identifier application number: M020

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
65112-304-01	65112030401	118 mL in 1 TUBE (65112-304-01)	118 ml	2004-06-01	No	No	Current