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 258 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Lip Balm SPF-15	ZINC OXIDE	TUBBY TODD	4d938672-5302-4e47-a582-c3e6467008cb	2024-12-18	Warnings	Exact identifier application number: M020
SaltyFace Daily Sun Shield Mineral Sunscreen For Face SPF 30	ZINC OXIDE	Saltyface Natural Inc	f0cc7ce9-81b3-439f-b5ee-96138de54e78	2024-12-18	Warnings	Exact identifier application number: M020
Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine	TITANIUM DIOXIDE, ZINC OXIDE	EK Clothing LLC dba Belasol	e999d752-6c00-459e-b6c3-d264c330597d	2024-12-18	Warnings	Exact identifier application number: M020
Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	EK Clothing LLC dba Belasol	f22626c1-0996-41d8-a2ec-3bf7491df657	2024-12-18	Warnings	Exact identifier application number: M020
Costa Sea Mineral Sunscreen SPF 50	ZINC OXIDE	COSTA SEA INC	841e1b3d-dbbc-4bb0-886a-fb2d077ae739	2024-12-18	Warnings	Exact identifier application number: M020
SPF 50 plus Sunscreen All Mineral Active Ingredients	TITANIUM DIOXIDE AND ZINC OXIDE	KAS Direct LLC dba BabyGanics	247aae3d-1845-4dd8-b774-b9e8214809a2	2024-12-18	Warnings	Exact identifier application number: M020
Softlips Vanilla, Watermelon, Cherry	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	2235d029-157e-4a30-be90-605e6bc143fd	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Salted Caramel, Candy Apple, Marshmallow Ghost	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	42cf4623-0eb8-455a-b374-8e17e9336b92	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Peppermint Mocha, Apple Chai Cider, Orange Cranberry	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	0338c078-695d-4d4e-9e90-5a8a98d49524	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Pearl Plus Vanilla	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	107bcaa9-4347-4979-be44-35183a9ee67e	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Raspberry	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	d18b4c19-0365-44ec-bea8-4328e537e0d8	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Watermelon	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	03062f13-270d-49cf-8939-2349f12e9cba	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Vanilla Watermelon	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	f733747a-ad1a-4222-baf1-69dcd90a3350	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Vanilla Watermelon	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	1fbe85a2-4cd7-45bd-85a2-83bbf75c5f97	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Marshmallow Ghost	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	8d55141d-5d6f-4eec-87dc-d3c808cf7a6a	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Pearl	OCTINOXATE, OCTISALATE	The Mentholatum Company	43e175b4-7a48-431e-bf27-9ce7dee53f5e	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Oasis Watermelon Blackberry	DIMETHICONE, OXYBENZONE, OCTINOXATE	The Mentholatum Company	e1213808-4dad-4fd0-871a-04bba094a3cc	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Peppermint	DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE	The Mentholatum Company	1a0062f1-fcfc-4d6a-8274-2ebbc5fbdb27	2024-12-17	Warnings	Exact identifier application number: M020
Softlips Oasis Pineapple Coconut, Peach Mango, Strawberry Kiwi	DIMETHICONE, OXYBENZONE, OCTINOXATE	The Mentholatum Company	7c8a4921-ae45-47fb-a64e-c72b1a386d0d	2024-12-17	Warnings	Exact identifier application number: M020
Mentholatum Medicated Lip Balm Cherry	DIMETHICONE, OCTINOXATE, OCTISALATE	The Mentholatum Company	6edb132d-bb67-4e6c-8e18-db0305073a71	2024-12-17	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