Oil-Free Daily Hydration SPF 15

Product NDC: 76151-105
11-digit product format: 761510105
Labeler code: 76151
Product ID: 76151-105_2d025da2-1f3a-2062-e063-6294a90ab9e9
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE, AVOBENZONE
Dosage form: CREAM
Route: TOPICAL
Labeler: Boscia LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-04-16
Substance: OCTINOXATE; AVOBENZONE
Active strength: 50; 30 mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 12 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
2025-02-02 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	76151-105-52	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	76151-105-11	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	76151-105-52	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	76151-105-11	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	76151-105-52	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	76151-105-11	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	76151-105-52	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	76151-105-11	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

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: Oil-Free Daily Hydration SPF 15
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	50 mg/mL
AVOBENZONE	30 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup
G63QQF2NOX	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
ec322ae5-ab03-4c7b-9c6d-0bda3327c72a	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
76151-105-11	2025-02-01	Oil-Free Daily Hydration SPF 15
76151-105-52	2025-02-01	Oil-Free Daily Hydration SPF 15
76151-105-11	2025-01-30	Oil-Free Daily Hydration SPF 15
76151-105-52	2025-01-30	Oil-Free Daily Hydration SPF 15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76151-105-11	Oil-Free Daily Hydration SPF 15	40 mL in 1 TUBE	CREAM	40		9
76151-105-52	Oil-Free Daily Hydration SPF 15	15 mL in 1 TUBE	CREAM	15		9

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
AVOBENZONE	ACTIVE INGREDIENT	G63QQF2NOX	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
AVOBENZONE	ACTIVE MOIETY	G63QQF2NOX	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
ALUMINUM HYDROXIDE	INACTIVE INGREDIENT	5QB0T2IUN0	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
ARCTIUM LAPPA ROOT	INACTIVE INGREDIENT	597E9BI3Z3	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
BUTYLENE GLYCOL	INACTIVE INGREDIENT	3XUS85K0RA	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
CITRUS AURANTIUM FLOWER	INACTIVE INGREDIENT	O730ZX2Z83	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP	INACTIVE INGREDIENT	08H094218D	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
HYDROXYETHYL CELLULOSE (140 CPS AT 5%)	INACTIVE INGREDIENT	8136Y38GY5	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
PENTYLENE GLYCOL	INACTIVE INGREDIENT	50C1307PZG	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
PHELLODENDRON AMURENSE BARK	INACTIVE INGREDIENT	PBG27B754G	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
POTASSIUM PHOSPHATE	INACTIVE INGREDIENT	B7862WZ632	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
ROSEMARY	INACTIVE INGREDIENT	IJ67X351P9	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1
ZINC OXIDE	INACTIVE INGREDIENT	SOI2LOH54Z	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76151-105	OIL-FREE DAILY HYDRATION SPF 15 (OCTINOXATE, AVOBENZONE) CREAM [BOSCIA LLC]	9	Current NDC, Legacy NDC, 2 package rows	20250201_ec322ae5-ab03-4c7b-9c6d-0bda3327c72a.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 69 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ALOE KOTE SPF 25	OCTINOXATE, OXYBENZONE, HOMOSALATE	Aloe Care International, LLC	12e78c53-ba19-4c8e-bd2f-8c85fccbc179	2026-01-26	Warnings	Exact identifier application number: M020
ALOE UP KIDS SPORT SUNSCREEN SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Aloe Care International, LLC	62016e94-b5d2-4ba2-ab9c-b0b2c1ead650	2026-01-26	Warnings	Exact identifier application number: M020
Homosalate 10 Avobenzone 3% Octocrylene 6%	SPF 45 FACE	S&C Hampton Sun LLC	e49808c9-5025-4965-8679-7fe824cf6907	2026-01-26	Warnings	Exact identifier application number: M020
ENVIRONMENTAL DEFENSE	ZINC OXIDE	Avasol LLC	1fbddab4-71f7-4167-ad21-30040b7c71bb	2026-01-26	Warnings	Exact identifier application number: M020
Surfers Barrier	ZINC OXIDE	Avasol LLC	d6e2ac0a-3bf6-4d08-8647-6a23de2ac857	2026-01-26	Warnings	Exact identifier application number: M020
SURFERS BARRIER SPF 50	ZINC OXIDE, TITANIUM DIOXIDE	Avasol LLC	ec55eef0-17e6-416d-bd5e-548f2f323cea	2026-01-26	Warnings	Exact identifier application number: M020
Zenskin Watery Dew Nia-Cica Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE SUNSCREEN	Zenskin Co. Ltd.	49584899-d523-9677-e063-6394a90a1403	2026-01-26	Warnings	Exact identifier application number: M020
Caring mill sun serum with Vitamin C Niacinamide	HOMOSALATE OCTOCRYLENE OCTISALATE AVOBENZONE	FSA Store lnc.	4931ee71-1088-1ac1-e063-6294a90ad82b	2026-01-25	Warnings	Exact identifier application number: M020
Caring mill Mineral Eye Cream	ZINC OXIDE	FSA STORE INC.	4932ea19-28cc-b245-e063-6394a90ac7aa	2026-01-25	Warnings	Exact identifier application number: M020
Ceile SPF 30 prime PROTECT Broad Spectrum SPF 30 Sunscreen	SUNSCREEN 30 MINERAL	LE COSMETICS INC	2cee0413-d532-c192-e063-6294a90aa823	2026-01-25	Warnings	Exact identifier application number: M020
BeginS by JUNGSAEMMOOL Blue Chamomile Hyaluronic Acid Aqua Sunscreen Broad Spectrum SPF 50 plus	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Jungsaemmool Beauty Co., Ltd.	62e23503-7233-434a-91f0-092f10d2717d	2026-01-24	Warnings	Exact identifier application number: M020
BeginS by JUNGSAEMMOOL Blue Chamomile Hyaluronic Acid Airy Sun Stick Broad Spectrum SPF 50 plus	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Jungsaemmool Beauty Co., Ltd.	030a20fb-4846-4a5c-9808-a399aac2ff0b	2026-01-24	Warnings	Exact identifier application number: M020
Mimosa Lane SPF45	OCTINOXATE, OCTISALATE, ZINC OXIDE SUNSCREEN	R&G Divergency LLC	40f3b8ea-bfa5-4c66-9c79-c4408bda857a	2026-01-24	Warnings	Exact identifier application number: M020
111 SKIN SUNSCREEN SPF 50	ZINC OXIDE	Bentley Laboratories, LLC	b1265797-71dd-4302-ab26-dbff6ccec856	2026-01-23	Warnings	Exact identifier application number: M020
Mania Holic Sunscreen Pack	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	Firstmarket Co., ltd.	b95a460c-1f7b-4193-b305-466e073af640	2026-01-23	Warnings	Exact identifier application number: M020
JAFRA ALWAYS LONG WEAR FOUNDATION BROAD SPECTRUM SPF 15 SUNSCREEN 320	HOMOSALATE,OCTISALATE,ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	1cdbae71-441b-426d-99ee-c889d76af452	2026-01-23	Warnings	Exact identifier application number: M020
JAFRA ALWAYS LONG WEAR FOUNDATION BROAD SPECTRUM SPF 15 SUNSCREEN 250	HOMOSALATE,OCTISALATE,ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	8f4b5e0a-4578-4af3-b7d9-a19d4eb732e7	2026-01-23	Warnings	Exact identifier application number: M020
ISA KNOX 365 BB SUNSCREEN Broad Spectrum SPF 40, PA	TITANIUM DIOXIDE	LG Household and Healthcare, Inc.	65e70306-9e79-494d-9217-a43002f16307	2026-01-23	Warnings	Exact identifier application number: M020
O HUI Sun Science Ideal Cover Sunscreen Broad Spectrum	TITANIUM DIOXIDE	LG Household and Healthcare, Inc.	c15ffd23-271d-458d-9048-9bc50331d5d7	2026-01-23	Warnings	Exact identifier application number: M020
Aqua protection Sunscreen Broad Spectrum SPF50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	ENGLEWOOD LAB, INC.	627e6ea5-016b-4ab6-a50c-aa9c27e5cca1	2026-01-23	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
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76151-105-11	76151010511	40 mL in 1 TUBE (76151-105-11)	40 ml	2017-12-19	0000-00-00	No	No	Current
76151-105-52	76151010552	15 mL in 1 TUBE (76151-105-52)	15 ml	2017-12-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Oil-Free Daily Hydration SPF 15	Boscia LLC \| Englewood Lab, Inc.	2025-01-31	HUMAN OTC DRUG LABEL	9