Everyday Sun Defense

Product NDC: 83580-010
11-digit product format: 835800010
Labeler code: 83580
Product ID: 83580-010_442002ff-619f-5d98-e063-6394a90ad32c
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Hommerejuvenate, Inc.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-04-01
Substance: ZINC OXIDE
Active strength: 9.4 g/9.4g
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: Everyday Sun Defense
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	9.4 g/9.4g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SOI2LOH54Z	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
05aa1a1a-9e4f-2781-e063-6394a90aef6b	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ef9a935e-31b7-402c-a66c-716cdfe4f126	Product name	9	20241218
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
115c5bd2-98e1-4a98-8292-90803ca7e851	Product name	1	20220127
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
f1e0dc7e-7d61-4625-b6d9-4894927679d7	Product name	2	20211025
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
e4870509-7e28-6f92-f0be-dd3dd889a9cf	Product name	5	20200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cd	Product name	2	20190619
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
684ea482-2e8b-14af-5664-b98f1e402036	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508
b060cc1a-fe47-856b-0b77-4448b5963de8	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83580-010-01	Everyday Sun Defense	60 g in 1 TUBE	CREAM	60		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83580-010	EVERYDAY SUN DEFENSE (ZINC OXIDE) CREAM [HOMMEREJUVENATE, INC.]	3	Current NDC, 1 package rows	20240402_05aa1a1a-9e4f-2781-e063-6394a90aef6b.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 228 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stay Ageless Tinted Mineral Sunscreen Broad Spectrum SPF30	TITANIUM DIOXIDE AND ZINC OXIDE	DERM ASSO. MID OHIO	2d04bc5d-6f11-4f56-e063-6294a90ae755	2025-01-31	Warnings	Exact identifier application number: M020
TiZO Mineral Sun Defense SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals Ltd.	2d0766a1-4091-e84a-e063-6394a90a004a	2025-01-31	Warnings	Exact identifier application number: M020
Hello Sunday The Shimmer One Mineral Glow SPF 45	ZINC OXIDE	Kao USA Inc.	0c935521-4e8b-0605-e063-6394a90a0bbc	2025-01-31	Warnings	Exact identifier application number: M020
Hello Sunday The Invisible One Sunscreen Plus Primer SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Kao USA Inc.	0c7ce5b9-5ab4-d845-e063-6394a90afa76	2025-01-31	Warnings	Exact identifier application number: M020
Hello Sunday The Mineral One Lightweight Serum SPF 50	ZINC OXIDE	Kao USA Inc.	0c91894f-a40e-73e9-e063-6394a90ab807	2025-01-31	Warnings	Exact identifier application number: M020
Hello Sunday The One Thats a Serum Hydrating Serum SPF 45	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Kao USA Inc.	0c913096-c000-4336-e063-6394a90a560c	2025-01-31	Warnings	Exact identifier application number: M020
Hello Sunday Bestseller Daily SPF Duo	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Kao USA Inc.	26cf264b-f68d-5691-e063-6394a90a8ab4	2025-01-31	Warnings	Exact identifier application number: M020
TiZO Ultra Zinc SPF 40 (Tinted)	ZINC OXIDE	Fallien Cosmeceuticals, LTD	2d0856cf-d3da-5a77-e063-6294a90ad5b4	2025-01-31	Warnings	Exact identifier application number: M020
FRE PROTECT BODY Ultra-Light Gel Cream SPF 50	ZINC OXIDE	Peer Pharm Ltd.	2cd83c55-851c-089e-e063-6294a90ad6bc	2025-01-30	Warnings	Exact identifier application number: M020
FRE BRONZE ME Sun-Kissed Mineral Sunscreen SPF 50	ZINC OXIDE	Peer Pharm Ltd.	2cd958a3-bad6-725e-e063-6294a90a8578	2025-01-30	Warnings	Exact identifier application number: M020
FRE PLUMP ME PEPTIDE LIP TINT CASSIS SPF 30	ZINC OXIDE	Peer Pharm Ltd.	2cd77d62-77df-f3a9-e063-6394a90ad57d	2025-01-30	Warnings	Exact identifier application number: M020
FRE PLUMP ME PEPTIDE LIP TINT PAMPELONNE SPF 30	ZINC OXIDE	Peer Pharm Ltd.	2caf3b6b-3a05-b24a-e063-6394a90a4799	2025-01-30	Warnings	Exact identifier application number: M020
Jil Goorman Skincare Sun Guard SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	SAN DIEGO NATURAL SOAP COMPANY	9a088bed-3b85-4bf5-923b-4c99eb904a8d	2025-01-30	Warnings	Exact identifier application number: M020
FRE PLUMP ME PEPTIDE LIP TINT MONACO SPF 30	ZINC OXIDE	Peer Pharm Ltd.	2baf0278-7e13-4db0-e063-6294a90ae9de	2025-01-30	Warnings	Exact identifier application number: M020
Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50	ZINC OXIDE	Babo Botanicals, Inc.	08a175ae-2307-ef8d-e063-6394a90ad234	2025-01-30	Warnings	Exact identifier application number: M020
Babo Botanicals Super Shield Mineral Sunscreen SPF50	ZINC OXIDE	Babo Botanicals, Inc	08b7bcfd-0c7c-a14f-e063-6294a90a7797	2025-01-30	Warnings	Exact identifier application number: M020
Salt and Stone Sunscreen Lip Balm SPF 30	ZINC OXIDE	Salt and Stone LLC	b555aa10-1547-63cc-e053-2995a90ad20d	2025-01-30	Warnings	Exact identifier application number: M020
COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR	OCTINOXATE, OCTISALATE, OXYBENZONE, AND TITANIUM DIOXIDE	Bluemercury	5c590aed-d2f2-4478-8919-37c848752b42	2025-01-29	Warnings	Exact identifier application number: M020
LiProtect SPF 35	ZINC OXIDE, TITANIUM DIOXIDE	Science of Skincare	0d0a2657-4098-3c60-e063-6294a90acabb	2025-01-29	Warnings	Exact identifier application number: M020
Perfect Sunscreen Tinted Mineral SPF50	ZINC OXIDE	Bluemercury, Inc.	4c978154-679f-472a-95ab-56878c5c70cd	2025-01-29	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83580-010-01	83580001001	60 g in 1 TUBE (83580-010-01)	60 g	2024-04-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Everyday Sun Defense	Hommerejuvenate, Inc. \| DERMACEUTICAL LABORATORIES LIMITED LIABILITY COMPANY	2025-11-21	HUMAN OTC DRUG LABEL	4