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 236 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Black Girl Sunscreen Sunscreen SPF 30 broad Spectrum	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Black Girl Sunscreen, LLC	2bc50182-30f5-b77e-e063-6394a90a6355	2025-01-15	Warnings	Exact identifier application number: M020
MEDIFORDEAR CICA CALMING SUNSCREEN	HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, AVOBENZONE	Youngwon Costech Co.,ltd.	2bc94923-b221-5159-e063-6394a90ab8ff	2025-01-15	Warnings	Exact identifier application number: M020
Meaningful Beauty Cindy Crawford Anti-Aging Day Creme with Environmental Protection Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OXYBENZONE	Meaningful Beauty, LLC	6423e1c7-85cd-46f8-8fc9-a7284e3577d1	2025-01-15	Warnings	Exact identifier application number: M020
Stay AgelessTinted Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	Spectrum Aesthetics Laser Training LLC	026b9b30-ef08-bf2e-e063-6394a90a54a6	2025-01-14	Warnings	Exact identifier application number: M020
Daily Sunscreen Broad Spectrum SPF 30 UVA UVB	MINERAL SUNSCREEN SPF 30	IHerb, LLC	2d8101ef-96a3-1463-e063-6294a90add4d	2025-01-14	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Tinted Mineral Sunscreen Face Stick Unscented SPF 30	ZINC OXIDE	9055-7588 Quebec Inc. DBA Attitude	0d85b0a1-3705-2829-e063-6394a90a0ed7	2025-01-13	Warnings	Exact identifier application number: M020
Attitude mineral sunscreen orange blossom SPF 30	ZINC OXIDE	9055-7588 Quebec Inc. DBA Attitude	0b85ea68-6113-4e92-a10a-39d13099d12d	2025-01-13	Warnings	Exact identifier application number: M020
Skinfuse Shield SPF 30	ZINC OXIDE	Owen Biosciences, Inc.	02d46d44-2476-4f96-9c72-783c392317de	2025-01-13		Exact identifier application number: M020
Chem Free SPF 30	ZINC OXIDE	Owen Biosciences, Inc.	7e5930fe-eb0f-4a21-8065-8831dd5b351c	2025-01-13	Warnings	Exact identifier application number: M020
Sheglam Dew and Done Skin Tint with SPF 20 Shell	ZINC OXIDE	EVER FAME PTE. LTD.	2b9b5a73-858e-78dd-e063-6394a90ad082	2025-01-13	Warnings	Exact identifier application number: M020
Tula Skincare protect and go dewy glow sunscreen stick broad spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	2b9acb63-b32c-336c-e063-6394a90a4a9c	2025-01-13	Warnings	Exact identifier application number: M020
Brush and Go All Skin types	TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE	Noon Aesthetics M.R. Ltd	9ee5b3c2-4369-4c4b-ab55-b52661b82188	2025-01-13	Warnings	Exact identifier application number: M020
Priia Tinted Mineral Sunscreen and Primer	TITANIUM DIOXIDE, ZINC OXIDE	Priia Cosmetics Inc	5c4219ac-d65f-43a5-8ec4-8732b9b344cf	2025-01-13	Warnings	Exact identifier application number: M020
Brush and Go Oily Problematic Skin	TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE	Noon Aesthetics M.R. Ltd	b4295453-f193-4bed-be5b-efcd91772107	2025-01-13	Warnings	Exact identifier application number: M020
Zealios SPF LipGuard	OCTISALATE AND AVOBENZONE	Personal Best Products Inc. dba Zealios	3a07822b-a7c9-40af-a8f7-bea591c7a49b	2025-01-13	Warnings	Exact identifier application number: M020
SPF-30 BB	ZINC OXIDE	ZION HEALTH	66d33d8c-8900-4698-98fe-0dedafe674d8	2025-01-13	Warnings	Exact identifier application number: M020
Priia Tinted Mineral Sunscreen and Primer	TITANIUM DIOXIDE, ZINC OXIDE	Priia Cosmetics Inc	b2addf27-9139-48b4-85e6-618f4b5311cc	2025-01-13	Warnings	Exact identifier application number: M020
Skin Apeel Ageless Defense SPF 40 Broad Spectrum	ZINC OXIDE	Skin Apeel, Inc.	c3bbe779-b012-4f19-8b90-2c7a4dd88617	2025-01-13	Warnings	Exact identifier application number: M020
UNCOMPLIKATED MAKEUP SETTING SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	KATE SOMERVILLE SKINCARE LLC	1a33cb41-440a-41cb-9832-24255bfa2b7c	2025-01-12	Warnings	Exact identifier application number: M020
ALLSWELL MINERAL SUNSCREEN SPF 30	ZINC OXIDE	Stream2Sea, LLC	03bee988-d6e3-4290-a926-9c5366649cba	2025-01-12	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