Hawaiian Natural Zinc Sunscreen SPF 50

Product NDC: 72096-101
11-digit product format: 720960101
Labeler code: 72096
Product ID: 72096-101_46b63682-0910-142e-e063-6394a90a403a
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Kokua Sun Care
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-02-10
Substance: ZINC OXIDE
Active strength: 25 g/100g
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 · 27 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	72096-101-02	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	72096-101-01	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	72096-101-02	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	72096-101-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72096-101-02	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72096-101-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72096-101-02	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72096-101-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72096-101-02	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72096-101-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72096-101-02	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72096-101-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
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	72096-101-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72096-101-01	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	72096-101-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72096-101-01	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	72096-101-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72096-101-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: Hawaiian Natural Zinc Sunscreen SPF 50
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	25 g/100g

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
64a5589b-735d-38ba-e053-2a91aa0ad8f4	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72096-101-01	2025-12-30	Kokua Hawaiian Natural Zinc Sunscreen SPF 50 (89 ml / 3 fl oz) (30 ml / 1 fl oz)
72096-101-02	2025-12-30	Kokua Hawaiian Natural Zinc Sunscreen SPF 50 (89 ml / 3 fl oz) (30 ml / 1 fl oz)
72096-101-01	2025-01-30	Kokua Hawaiian Natural Zinc Sunscreen SPF 50 (89 ml / 3 fl oz) (30 ml / 1 fl oz)
72096-101-02	2025-01-30	Kokua Hawaiian Natural Zinc Sunscreen SPF 50 (89 ml / 3 fl oz) (30 ml / 1 fl oz)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72096-101-01	Hawaiian Natural Zinc Sunscreen SPF 50	89 g in 1 BOX	LOTION	89		5
72096-101-02	Hawaiian Natural Zinc Sunscreen SPF 50	30 g in 1 BOX	LOTION	30		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72096-101	HAWAIIAN NATURAL ZINC SUNSCREEN SPF 50 (ZINC OXIDE) LOTION [KOKUA SUN CARE]	4	Current NDC, Legacy NDC, 2 package rows	20230630_64a5589b-735d-38ba-e053-2a91aa0ad8f4.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 108 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
First Aid Beauty FAB Ultra Repair Face Moisturizer with Sunscreen Broad Spectrum SPF 30	OCTOCRYLENE, AND ZINC OXIDE	The Procter & Gamble Manufacturing Company	f6801575-6081-7566-e053-2995a90a20a8	2025-12-18	Warnings	Exact identifier application number: M020
Olay Regenerist Regenerating with Sunscreen Broad Spectrum SPF 15	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	00280745-908b-468f-e063-6294a90aa12f	2025-12-18	Warnings	Exact identifier application number: M020
OLAY Prime plus Protect Facial Sunscreen with Vitamin C SPF35 Matte Finish	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	10bd41ac-9b96-840d-e063-6394a90a98d9	2025-12-18	Warnings	Exact identifier application number: M020
Olay Glow plus Protect Sunscreen Dewy Glow SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	The Procter & Gamble Manufacturing Company	10bc4127-7569-d0de-e063-6294a90a97bf	2025-12-18	Warnings	Exact identifier application number: M020
First Aid Beauty FAB Hydrating Sunscreen Milk Broad Spectrum SPF 45	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	29645d90-a444-4090-e063-6294a90ac7e3	2025-12-18	Warnings	Exact identifier application number: M020
Skin On Skin BC Foundation SPF 40 - Tan Golden	OCTISALATE, HOMOSALATE, ZINC OXIDE	YENSA Beauty, LLC	46440bac-de69-e59c-e063-6394a90a76c0	2025-12-18	Warnings	Exact identifier application number: M020
FUSIDYNE DERMA TROUBLE Zinc Calming Sunscreen	ZINC OXIDE	DONG WHA PHARM. CO., LTD.	46457c78-74d6-ea6a-e063-6294a90a24ac	2025-12-18	Warnings	Exact identifier application number: M020
THE MUG GUARD Invisible Gel Suncare for Face	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Dune Suncare, Inc.	4646988c-1060-ed5f-e063-6394a90aa765	2025-12-18	Warnings	Exact identifier application number: M020
Sage and Zinc Facial Hydrating SPF15	ZINC OXIDE	Emeis Cosmetics Pty Ltd	ccabd647-ecdd-7230-e053-2a95a90a7a96	2025-12-18	Warnings	Exact identifier application number: M020
Avail Facial Sunscreen SPF 25	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	Emeis Cosmetics Pty Ltd	7be903e4-5f07-35b2-e053-2991aa0a1340	2025-12-17	Warnings	Exact identifier application number: M020
Mineral Sheer Stick	ZINC OXIDE	Supergoop, LLC	0beed72e-51df-d15a-e063-6394a90af559	2025-12-17	Warnings	Exact identifier application number: M020
Sunscreen Lotion118ml	ZINC OXIDE 12%,TITANIUM DIOXIDE 6%, HOMOSALATE 14%,OCTISALATE 5%	Foshan Sugar Max Cosmetics CO.,Ltd	4620c41a-2188-00f5-e063-6394a90a613c	2025-12-17	Warnings	Exact identifier application number: M020
Sunscreen Cream	ZINC OXIDE 15%,TITANIUM DIOXIDE 6%,HOMOSALATE 5%,OCTISALATE 4%	Foshan Sugar Max Cosmetics CO.,Ltd	46224dbe-a0fb-c242-e063-6394a90a2634	2025-12-17	Warnings	Exact identifier application number: M020
CAPTURE TOTALE C.E.L.L. ENERGY SUPER POTENT SERUM FOUNDATION BROAD SPECTRUM SPF 20 0N	ENSULIZOLE, OCTISALATE	Parfums Christian Dior	31141a45-54e2-4463-ab42-4df56d911650	2025-12-17	Warnings	Exact identifier application number: M020
Perricone High Potency Face Finishing and Firming Moisturizer	TITANIUM DIOXIDE, ZINC OXIDE	THG Beauty USA LLC	2409cea1-7077-dc12-e063-6294a90a4558	2025-12-17	Warnings	Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Glow Advanced Skin and Body Care, LLC	3635a073-5484-f96c-e063-6394a90adef5	2025-12-17		Exact identifier application number: M020
Mineral Sunscreen Lip	TITANIUM DIOXIDE, ZINC OXIDE	Glow Advanced Skin and Body Care, LLC	36362dc7-31d7-f766-e063-6294a90a129b	2025-12-17		Exact identifier application number: M020
Mineral Sunscreen Non-Tinted	ZINC OXIDE	Glow Advanced Skin and Body Care, LLC	3635e45b-6978-ac69-e063-6294a90a22ac	2025-12-17		Exact identifier application number: M020
Prime and Protect	TITANIUM DIOXIDE, ZINC OXIDE	Shannon Cornelsen-Lewandowski	36480f7f-37e8-decd-e063-6394a90ada60	2025-12-17		Exact identifier application number: M020
Prime and Protect	TITANIUM DIOXIDE, ZINC OXIDE	Shannon Cornelsen-Lewandowski	364827bd-5781-eb53-e063-6394a90ab22f	2025-12-17		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
72096-101-01	72096010101	89 g in 1 BOX (72096-101-01)	89 g	2018-02-10	0000-00-00	No	No	Current
72096-101-02	72096010102	30 g in 1 BOX (72096-101-02)	30 g	2023-06-12		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Kokua Hawaiian Natural Zinc Sunscreen SPF 50 (89 ml / 3 fl oz) (30 ml / 1 fl oz)	Kokua Sun Care \| Columbia Cosmetics Manufacturing, Inc.	2025-12-29	HUMAN OTC DRUG LABEL	5