doTERRA sun

Product NDC: 71630-173
11-digit product format: 716300173
Labeler code: 71630
Product ID: 71630-173_2ccc91ed-555f-fb8f-e063-6394a90a96da
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: SPRAY
Route: TOPICAL
Labeler: doTERRA International, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-09-01
Substance: ZINC OXIDE
Active strength: 17.5 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 · 18 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
2025-02-02 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	71630-173-17	`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	71630-173-17	`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	71630-173-17	`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	71630-173-17	`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	71630-173-17	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	71630-173-17	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	71630-173-17	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	71630-173-17	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	71630-173-17	`1332a3947898…`	`d4bfe170f9cd…`

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: doTERRA sun
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	17.5 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
da5c48d6-1859-983d-e053-2a95a90a4c3e	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71630-173-17	2025-02-05	C162847	48780-1	1030e365-04e3-111a-e063-dadaa90a10e2	doTERRA Sun Body Mineral Sunscreen Spray
71630-173-17	2024-01-30	C162847	48780-1	1030e365-04e3-111a-e063-dadaa90a10e2	doTERRA Sun Body Mineral Sunscreen Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71630-173-17	doTERRA sun	170 g in 1 BOTTLE, SPRAY	SPRAY	170		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71630-173	DOTERRA SUN (ZINC OXIDE) SPRAY [DOTERRA INTERNATIONAL, LLC]	2	Current NDC, Legacy NDC, 1 package rows	20250207_da5c48d6-1859-983d-e053-2a95a90a4c3e.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 133 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Daily Sun Defense	TITANIUM DIOXIDE, ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750c2fd-c5cc-fd00-e063-6394a90aeb89	2025-12-11	Exact identifier application number: M020
Non Tinted Ultra Zinc Face and Body	ZINC OXIDE	LIV BODY AND BEAUTY LLC	3750ffbf-a82d-b4b9-e063-6294a90a7d68	2025-12-11	Exact identifier application number: M020
The Block	ZINC OXIDE	ELITE ESTHETICS BY NICOLE CAROLINE LLC	34a6b17e-6e9e-3f2c-e063-6294a90a1c32	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum Non-Tinted	ZINC OXIDE	Teton Dermatology Holdings, Inc.	35093797-008b-b265-e063-6294a90a9949	2025-12-11	Exact identifier application number: M020
Tinted Zinc Protection	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3508d5a8-9d3c-51d1-e063-6394a90abc8e	2025-12-11	Exact identifier application number: M020
SPF 40 Broad Spectrum	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	35081ce0-2203-ab86-e063-6294a90aefd5	2025-12-11	Exact identifier application number: M020
Antioxidant SPF	ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509a916-f3e1-9c53-e063-6394a90a5bff	2025-12-11	Exact identifier application number: M020
Ultimate Physical Sunscreen Tinted	ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bb4953-ca8c-e927-e063-6394a90a1a31	2025-12-11	Exact identifier application number: M020
Lip Protection	TITANIUM DIOXIDE, ZINC OXIDE	Teton Dermatology Holdings, Inc.	3509eea7-f966-2080-e063-6294a90aeeb5	2025-12-11	Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bce44e-d9f4-9279-e063-6394a90a6453	2025-12-11	Exact identifier application number: M020
Ultimate Physical Sunscreen	ZINC OXIDE	HALEM DERMATOLOGY PLLC	35bc5ff5-8eb8-54cf-e063-6394a90ae3c2	2025-12-11	Exact identifier application number: M020
Tinted Mineral Daily Sunscreen	TITANIUM DIOXIDE ,ZINC OXIDE	Jordan Macall Acne & Anti-Aging Skincare LLC	350ad191-e51c-083d-e063-6394a90aa646	2025-12-11	Exact identifier application number: M020
Ultimate Physical Sunscreen	ZINC OXIDE	HALEM DERMATOLOGY PLLC	35be5dc0-861f-3738-e063-6394a90a23ca	2025-12-11	Exact identifier application number: M020
Tinted Mineral Daily Sunscreen	TITANIUM DIOXIDE ,ZINC OXIDE	Jordan Macall Acne & Anti-Aging Skincare LLC	350b2246-6e00-38fc-e063-6294a90ae382	2025-12-11	Exact identifier application number: M020
Calming Protection SPF40	ZINC OXIDE	FRESH FACED SKIN CARE LLC	35d0c081-67b4-ce46-e063-6294a90ad822	2025-12-11	Exact identifier application number: M020
Tinted Facial Protection SPF40	TITANIUM DIOXIDE, ZINC OXIDE	FRESH FACED SKIN CARE LLC	35d08e2a-b118-8634-e063-6294a90a918d	2025-12-11	Exact identifier application number: M020
Total Body Block Sunscreen	ZINC OXIDE	THE COMPLEXIONIST	38f53f6a-8e68-e30f-e063-6394a90afef2	2025-12-11	Exact identifier application number: M020
Fair Skin Anti-Aging	ZINC OXIDE	DERMOPERFECTION SKINCARE SERVICES, LLC	351bb329-90ea-f19a-e063-6394a90af107	2025-12-11	Exact identifier application number: M020
Oil Free Anti-Aging	ZINC OXIDE	DERMOPERFECTION SKINCARE SERVICES, LLC	351b4870-d9bd-c356-e063-6394a90a7763	2025-12-11	Exact identifier application number: M020
Anti-Aging Sun Protection NT	TITANIUM DIOXIDE, ZINC OXIDE	DERMOPERFECTION SKINCARE SERVICES, LLC	351a20df-bd8a-8ea6-e063-6294a90abaaf	2025-12-11	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
71630-173-17	71630017317	170 g in 1 BOTTLE, SPRAY (71630-173-17)	170 g	2022-09-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
doTERRA Sun Body Mineral Sunscreen Spray	doTERRA International, LLC	2025-01-28	HUMAN OTC DRUG LABEL	2