Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30

Product NDC: 72096-102
11-digit product format: 720960102
Labeler code: 72096
Product ID: 72096-102_46b79953-4c5f-921b-e063-6394a90a875f
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Kokua Sun Care
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-04-18
Substance: ZINC OXIDE
Active strength: 18 g/100mL
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 · 22 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	72096-102-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	72096-102-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72096-102-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72096-102-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72096-102-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72096-102-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72096-102-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72096-102-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72096-102-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	72096-102-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	72096-102-01	`367a005e9d99…`	`383a685ebd0f…`

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 Broad Spectrum Tinted SPF 30
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	18 g/100mL

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
f9a12dac-2fd0-798f-e053-6394a90aa784	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72096-102-01	2025-12-30	C162847	48780-1	1030e365-0257-111a-e063-dadaa90a10e2	Kokua Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30 (89 ml / 3 fl oz)
72096-102-01	2024-07-30	C162847	48780-1	1030e365-0257-111a-e063-dadaa90a10e2	Kokua Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30 (89 ml / 3 fl oz)
72096-102-01	2024-01-30	C162847	48780-1	1030e365-0257-111a-e063-dadaa90a10e2	Kokua Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30 (89 ml / 3 fl oz)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72096-102-01	Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30	89 mL in 1 BOTTLE	CREAM	89		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72096-102	HAWAIIAN NATURAL ZINC SUNSCREEN BROAD SPECTRUM TINTED SPF 30 (ZINC OXIDE) CREAM [KOKUA SUN CARE]	1	Current NDC, 1 package rows	20230623_f9a12dac-2fd0-798f-e053-6394a90aa784.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 184 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sun Kids mineral STRAWBERRY SUNSCREEN BROAD SPECTRUM SPF 50	ZINC OXIDE	The Natural SKN Company	400c67aa-55a6-67ea-e063-6294a90a0213	2025-09-30	Warnings	Exact identifier application number: M020
toty Ilumina CC Creamy Compact Refill 1C	TITANIUM DIOXIDE	Chipican LLC	f0596830-77ed-11f0-e053-2995a90a8ff5	2025-09-29	Warnings	Exact identifier application number: M020
U V-Lamp Shield Mani-Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD	3fe7e1c3-e6cd-1420-e063-6394a90a4138	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	053e76f0-8ca0-645d-e063-6394a90a01d2	2025-09-28	Warnings	Exact identifier application number: M020
Hawaiian Tropic Mineral Translucent Sunscreen Powder SPF 30	ZINC OXIDE	Edgewell Personal Care Brands LLC	cdc54f23-0efb-2fb4-e053-2995a90ae58b	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	0540017a-52ac-7972-e063-6394a90a139c	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	08f3b27f-b233-d406-e063-6394a90ada76	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	128a3772-b9b7-0d10-e063-6294a90a3e05	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	203c82a2-0131-8023-e063-6294a90aba7b	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	203c780a-3107-d71a-e063-6394a90aca25	2025-09-28	Warnings	Exact identifier application number: M020
HAWAIIAN TROPIC	AVOBENZONE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	31d01fae-4085-d84a-e063-6294a90ab981	2025-09-28	Warnings	Exact identifier application number: M020
Hawaiian Tropic	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands, LLC	3388c2fa-8082-95d4-e063-6294a90a94b8	2025-09-28	Warnings	Exact identifier application number: M020
Neutrogena Beach Defense Water Plus Sun Protection Sunscreen Broad Spectrum SPF30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	Kenvue Brands LLC	b10a7794-7e4f-412b-9eb2-773107ecb7fc	2025-09-26	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50	HOMOSALATE 10.00% OCTOCRYLENE 10.00% OCTISALATE 5.00% AVOBENZONE 3.00%	Black Girl Sunscreen	fed22570-e0ae-43e1-b6ce-1f0ad01684c3	2025-09-26	Warnings	Exact identifier application number: M020
Sun Glazed SPF 30 Sunscreen Glow Oil	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	Baxter Laboratories Pty. Ltd.	3fa41ed1-2f7f-18e6-e063-6294a90a0a8b	2025-09-25	Warnings	Exact identifier application number: M020
Smooth Even Glow	TINTED SUNSCREEN BROAD SPF30	SKNVcare, LLC	3fa48151-fcb9-3d35-e063-6394a90a2eb6	2025-09-25	Warnings	Exact identifier application number: M020
CHEEK CREME BROAD SPECTRUM SPF 30 SUNSCREEN BLUSH HEAT WAVE	AVOBENZONE, HOMOSALATE, OCTISALATE	MDSolarSciences	3fa810b0-0211-f2a7-e063-6294a90a0b72	2025-09-25	Warnings	Exact identifier application number: M020
SUN BUFF SPF 30 MINERAL SUNSCREEN	ZINC OXIDE/TITANIUM DIOXIDE	SPF Ventures, LLC	3f874062-ebab-8993-e063-6294a90abfc5	2025-09-24	Warnings	Exact identifier application number: M020
HygieneLab Face and Body Mineral Sunscreen SPF 50	ZINC OXIDE	HYGIENELAB, INC	7db103da-b434-433a-a18f-a727165640c0	2025-09-24	Warnings	Exact identifier application number: M020
Eve Lom Daily Protection Broad Spectrum SPF 50 Sunscreen	HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTINOXATE AND OCTOCRYLENE	Space Brands Limited	0e2c9ffb-036d-49c5-abdb-2ee8888df318	2025-09-24	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
72096-102-01	72096010201	89 mL in 1 BOTTLE (72096-102-01)	89 ml	2023-04-18	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30	Kokua Sun Care \| Columbia Cosmetics Manufacturing, Inc.	2025-12-29	HUMAN OTC DRUG LABEL	2