TiZO Eye Renewal SPF 20 (Non-Tinted)

Product NDC: 58892-113
11-digit product format: 588920113
Labeler code: 58892
Product ID: 58892-113_24c33b97-e472-feca-e063-6394a90ad7d9
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Fallien Cosmeceuticals, LTD
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-09-01
Substance: ZINC OXIDE
Active strength: 90 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: TiZO Eye Renewal SPF 20 (Non-Tinted)
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	90 mg/g

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
33f8760c-2953-44a6-9239-424fdb97a5b3	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7dea7767-9f52-b60a-5435-33cb9cc28bae	Product name	4	20250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4	Product name	7	20250116
0ca83774-3f79-b837-5d6f-c210102f3bc8	Product name	6	20250114
41b814f3-0166-1c53-c9ef-a0794c7daf9d	Product name	3	20221110
a590be26-846c-8659-a5a1-fb25907965dc	Product name	2	20221110
2dc76302-91c0-4c35-ad78-99adfb049c4b	Product name	1	20200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2b	Product name	2	20180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
332e86c3-7875-ca6e-f934-2206d2b31996	Product name	1	20140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21	Product name	1	20140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508
d223c173-c39b-d764-47d4-d671d3088815	Product name	1	20140508
e01133ad-4dcd-c7f3-454b-2ff569ee160a	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
58892-113-15	TiZO Eye Renewal SPF 20 (Non-Tinted)	15 g in 1 BOTTLE, PUMP	CREAM	15	3
58892-113-15	TiZO Eye Renewal SPF 20 (Non-Tinted)	1 in 1 CARTON	CREAM	1	3
58892-113-05	TiZO Eye Renewal SPF 20 (Non-Tinted)	1.5 g in 1 PACKET	CREAM	1.5	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58892-113	TIZO EYE RENEWAL SPF 20 (NON-TINTED) (ZINC OXIDE) CREAM [FALLIEN COSMECEUTICALS, LTD]	3	Current NDC, Legacy NDC, 2 package rows	20241020_33f8760c-2953-44a6-9239-424fdb97a5b3.zip
58892-113	TIZO EYE RENEWAL SPF 20 (NON-TINTED) (ZINC OXIDE) CREAM [FALLIEN COSMECEUTICALS, LTD]	1	Current NDC, Legacy NDC, 1 package rows	20250212_2d40099a-2cfa-1d99-e063-6394a90a36a6.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 46 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Arizona Sun Kids Sunscreen SPF 30	SUNSCREEN	Arizona Sun Products	10f60367-6681-a589-e063-6394a90a6bb8	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Sunscreen Water Resistant SPF 30	SUNSCREEN	Arizona Sun Products	115b4d4c-51f1-ad62-e063-6294a90a3e53	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Sunscreen SPF 30	SUNSCREEN	Arizona Sun Products	10e48195-7bae-2422-e063-6394a90a261c	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Sunscreen SPF 30	SUNSCREEN	Arizona Sun Products	10e276e4-81f1-9429-e063-6394a90a800d	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Sunscreen SPF 8	SUNSCREEN	Arizona Sun Products	106a9608-f7a4-0f8c-e063-6394a90a26ab	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Bikerblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fced72-39f9-f3a3-e063-6294a90a8b73	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Golfblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fc2a82-260c-7cd3-e063-6394a90af2c1	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Cycleblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fd9aa5-dbd6-e5a7-e063-6394a90a3eac	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Golfblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fc93a7-f5be-965d-e063-6394a90ab335	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Bikerblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fd1661-1b91-b65b-e063-6394a90af89b	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Lipkist Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fbcb81-2735-53c8-e063-6394a90ab0fa	2026-04-09	Warnings	Exact identifier application number: M020
Arizona Sun Products Cycleblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fd8776-99f8-e5a4-e063-6394a90a2033	2026-04-09	Warnings	Exact identifier application number: M020
uLOOK Sunscreen SPF 50	SUNSCREEN	HAMEX GLOBAL COSMETICS LLC	4e05588c-486b-60e0-e063-6294a90af457	2026-04-09	Warnings	Exact identifier application number: M020
Pro-Tect Sports Sunscreen SPF 20	MERADIMATE, OCTINOXATE, OCTISALATE, OXYBENZONE	ABBE Laboratories, Inc.	35869e8d-8e48-4b22-8af3-6964fe8ac182	2026-04-09	Warnings	Exact identifier application number: M020
Sunright 50	AVOBENZONE, HOMOSALATE, AND OCTINOXATE	NSE Products, Inc.	b1b76481-da23-427f-9b34-b987019fa532	2026-04-09	Warnings	Exact identifier application number: M020
ThinkBaby SPF 30	ZINC OXIDE	thinkOperations,LLC	06862b00-c937-41af-ab5d-cea34160d035	2026-04-09	Warnings	Exact identifier application number: M020
Nutricentials Day Dream Protective	HOMOSALATE, OCTISALATE, AVOBENZONE, AND OCTOCRYLENE	NSE Products, Inc.	4a376e93-85e8-40a5-8641-d3e3d11fdeea	2026-04-08	Warnings	Exact identifier application number: M020
AGE20S UV MINERAL PRIMING SUNSCREEN	ZINC OXIDE	Aekyung Industrial Co., Ltd.	43c1f70b-0664-40be-e063-6394a90a2b48	2026-04-08	Warnings	Exact identifier application number: M020
AGE20S SUNSCREEN DUO	ZINC OXIDE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Aekyung Industrial Co., Ltd.	4eef11cd-85a1-0e44-e063-6394a90a5d44	2026-04-08	Warnings	Exact identifier application number: M020
Neutrogena MINERAL UV TINT FACE DEEP SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Acupac Packaging, Inc.	4ef430e8-cdc8-2897-e063-6394a90a3ac7	2026-04-08	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	Marketing end	Sample	Exclude flag	Status
58892-113-05	58892011305	1.5 g in 1 PACKET (58892-113-05)	1.5 g	2020-09-01		Yes	No	Current
58892-113-15	58892011315	1 BOTTLE, PUMP in 1 CARTON (58892-113-15) / 15 g in 1 BOTTLE, PUMP		2020-09-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Zinc Oxide - Fallien Cosmeceuticals, LTD \| Fragrance Manufacturing Inc. \| Custom Analytics LLC	Fallien Cosmeceuticals, LTD \| Fragrance Manufacturing Inc. \| Custom Analytics LLC	2025-02-03	HUMAN OTC DRUG LABEL	1
Zinc Oxide - Fallien Cosmeceuticals, LTD \| Custom Analytics LLC \| Fragrance Manufacturing Inc. (FMI)	Fallien Cosmeceuticals, LTD \| Custom Analytics LLC \| Fragrance Manufacturing Inc. (FMI)	2024-10-18	HUMAN OTC DRUG LABEL	3