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 61 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Broad Spectrum Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE	Meijer, Inc.	c76f5639-bd0f-4987-8c70-224ee33bbbad	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Meijer, Inc.	8795b9a7-1938-4dd9-92ad-3c044feae1da	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M020
Avobenzone, Homosalate, Octisalate	AVOBENZONE, HOMOSALATE, OCTISALATE	Meijer, Inc.	3f8bad95-8071-47b1-88a7-3a3f09f097b5	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M020
UV RESTORE FACE SERUM SUNSCREEN SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	BETTER INNOVATION LTD	4b9a881a-835b-ef0c-e063-6394a90a94af	2026-02-24	Warnings	Exact identifier application number: M020
MISTINE UV DEFENSE FACE MOISTURIZER SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BETTER INVENTION LTD	4b9a9303-662f-9614-e063-6294a90a6b51	2026-02-24	Warnings	Exact identifier application number: M020
SANTAL BLOOM SUNSCREEN BODY BROAD SPECTRUM SPF 50	SUNSCREEN	Saltair Body LLC	4b9ac780-ef7d-42fc-e063-6394a90ad62f	2026-02-24	Warnings	Exact identifier application number: M020
PINK BEACH SUNSCREEN BODY BROAD SPECTRUM SPF 50	SUNSCREEN	Saltair Body LLC	4b9b36a6-4da9-8439-e063-6394a90aa86b	2026-02-24	Warnings	Exact identifier application number: M020
SHISEIDO URBAN ENVIRONMENT MINERAL CLEAR SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	Shiseido Americas Corporation	b93f10dc-193d-4cda-94b6-3f0e54d89f21	2026-02-23	Warnings	Exact identifier application number: M020
cle de peau BEAUTE ADVANCED PROTECTIVE DAY	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Shiseido Americas Corporation	710975d8-43bf-40b9-82c2-d4dc2988956d	2026-02-23	Warnings	Exact identifier application number: M020
SHISEIDO ULTIMATE SUN PROTECTOR MINERAL	TITANIUM DIOXIDE AND ZINC OXIDE	SHISEIDO AMERICAS CORPORATION	5e31eee8-6532-47ea-99fc-22418791804b	2026-02-23	Warnings	Exact identifier application number: M020
Eryfotona Ageless	ZINC OXIDE	ISDIN Corp.	a58ac2ed-31b7-4a86-83ca-7630b0c9ea6f	2026-02-23	Warnings	Exact identifier application number: M020
Perfect Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SKIN PERFECT MEDICAL	4b47e7cb-17d6-6a7c-e063-6294a90abbea	2026-02-20	Warnings	Exact identifier application number: M020
Beauty Hydrating	HOMOSALATE, ZINC OXIDE	Meijer, Inc.	69b72139-757f-476d-99d2-33f5524c41d2	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M020
daily moisturizer	AVBENZONE, OCTISALATE, OCTOCRYLENE	Meijer, Inc.	6d301146-46e0-445c-b14e-3ec8ce76cb45	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Meijer, Inc.	e9f4a2bb-d21e-4b38-9a37-23c23c8ad857	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M020
Inkeeze Tattoo Products Hi-Definition Tattoo Sunscreen SPF 50 Coconut Scent	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Ink-eeze	3f759bec-4e33-46fa-a800-fa3a17d63df9	2026-02-19	Warnings	Exact identifier application number: M020
Allay Skin Solutions Protect Nourish Mineral Sunscreen SPF 42	TITANIUM DIOXIDE, ZINC OXIDE	ALLAY SKIN SOLUTIONS LLC	425bf1d7-f2cf-4237-9047-dd53054acd1c	2026-02-18	Warnings	Exact identifier application number: M020
e.l.f. Best and Obsessed Skincare Set	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	4b1c1150-5ac5-4a8b-e063-6394a90a5410	2026-02-18	Warnings	Exact identifier application number: M020
Hermes Plein Air-Baume de Teint Perfecteur Naturel-Enhancing Complexion Balm 85 TAMARIN	TITANIUM DIOXIDE	S.A. COMPTOIR NOUVEAU DE LA PARFUMERIE	dacff3dc-49d7-6416-e053-2a95a90a85c6	2026-02-18	Warnings	Exact identifier application number: M020
Degree Clinical	COOL RUSH INVISIBLE SOLID 96H ANTIPERSPIRANT DEODORANT	Conopco Inc. d/b/a/ Unilever	4b1f9fd3-3c49-9a98-e063-6294a90a20e0	2026-02-18	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
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