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 85 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daily Dose Bioretinol Mineral SPF 40	ZINC OXIDE	Supergoop, LLC	eb5bbc70-dbdf-06a8-e053-2995a90a66c1	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Body SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ec1c30bd-76e1-9d00-e053-2a95a90a1759	2026-01-09	Warnings	Exact identifier application number: M020
Glow Screen SPF 40	AVOBENZONE, OCTISALATE, OCTOCYLENE	Supergoop, LLC	21569637-332a-461b-bf6c-33af6a83a155	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 - Dawn	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f07145d5-b74d-7757-e053-2a95a90ac4c0	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 -Sunset	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f7e493da-8fc6-191d-e053-6294a90aa483	2026-01-09	Warnings	Exact identifier application number: M020
Supergoop Glow Screen SPF 40 Shade 2 Golden Hour	BROAD SPECTRUM SUNSCREEN	Supergoop LLC	d2928dd7-a813-4929-e053-2a95a90aaeb4	2026-01-09	Warnings	Exact identifier application number: M020
Superscreen Hydrating Daily Cream SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ff0e4e97-8f01-bd36-e053-6394a90a47ae	2026-01-09	Warnings	Exact identifier application number: M020
Lipshade SPF 30 Hey Yall	ZINC OXIDE	Supergoop, LLC	f93dfa13-ff18-ee38-e053-6394a90aea46	2026-01-09	Warnings	Exact identifier application number: M020
Triple Prep SPF 40	AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE	Supergoop, LLC	004df4e5-dba9-6030-e063-6394a90a76d3	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Lip Protector SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	12605fb4-0de6-94f3-e063-6294a90a3a6f	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Stick SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	2735c5c7-a4ef-33c3-e063-6294a90abf97	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Sunscreen SPF 50	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	Supergoop LLC	2860d42c-d644-8b5a-e063-6394a90aec10	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Mineral SPF 30 with Green Algae	ZINC OXIDE	Supergoop LLC	29a1ff4b-3875-5275-e063-6394a90a53fd	2026-01-09	Warnings	Exact identifier application number: M020
Every. Single. Face. Watery SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	d086a9b8-19e5-f713-e053-2995a90aa976	2026-01-09	Warnings	Exact identifier application number: M020
3D Tinted Moisturizing BS SPF 30	ZINC OXIDE	Allure Labs	47fd415f-819e-bbb8-e063-6394a90a2c6a	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE BODY SUNSCREEN SPF50	SUNCARE BODY SUNSCREEN SPF50	Aopline Biotechnology (Guangzhou) Co., Ltd.	4801cfd2-1fe2-d118-e063-6294a90a6c8b	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE BODY SUNSCREEN SPF30	SUNCARE BODY SUNSCREEN SPF30	Aopline Biotechnology (Guangzhou) Co., Ltd.	48026f09-6d15-8fa6-e063-6294a90a17cb	2026-01-09	Warnings	Exact identifier application number: M020
RODAN and FIELDS ENHANCEMENTS MEDIUM	TITANIUM DIOXIDE, ZINC OXIDE	Bentley Laboratories, LLC	6aa6ad3f-2c52-4031-9e6c-7526c42de71d	2026-01-09	Warnings	Exact identifier application number: M020
FACE SPF 47 SETTING	FACE SPF 47 SETTING SPRAY	Aopline Biotechnology (Guangzhou) Co., Ltd.	47db9a54-c02f-d2ea-e063-6394a90ab973	2026-01-08	Warnings	Exact identifier application number: M020
BADABOOM SUNSCREEN	SUNSCREEN	Aopline Biotechnology (Guangzhou) Co., Ltd.	47dbf363-2892-4530-e063-6294a90abe1f	2026-01-08	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
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