Pipette Mineral Sunscreen Broad Spectrum

Product NDC: 73517-382
11-digit product format: 735170382
Labeler code: 73517
Product ID: 73517-382_ec975c9d-a14e-db6c-e053-2995a90a9e8f
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Amyris, Inc
Application: M020
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2020-06-01
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 20 g/100mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	73517-382		I	Inactivated by FDA	2026-10-20
excluded package	package	73517-382	73517-382-01	I	Inactivated by FDA	2026-10-20
excluded package	package	73517-382	73517-382-02	I	Inactivated by FDA	2026-10-20
excluded package	package	73517-382	73517-382-03	I	Inactivated by FDA	2026-10-20

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 · 36 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	73517-382-01	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	73517-382-03	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	73517-382-02	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	73517-382-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	73517-382-03	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	73517-382-02	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	73517-382-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	73517-382-03	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	73517-382-02	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	73517-382-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	73517-382-03	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	73517-382-02	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	73517-382-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	73517-382-03	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	73517-382-02	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	73517-382-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	73517-382-03	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	73517-382-02	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	73517-382-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	73517-382-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	73517-382-03	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	73517-382-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73517-382-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73517-382-03	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	73517-382-02	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73517-382-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73517-382-03	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f47a510b-6679-4664-b2d6-47b5c4afe7cc	Product name	4	20260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61c	Product name	2	20250515
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
190f2a5b-bbc8-65c7-fcb0-97891307b917	Product name	1	20140508
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
73517-382-01	2025-01-30	C162847	48780-1	2cef2736-a2bd-d83d-e063-dadaa90ab31f	a93cd61a-ae83-4c45-8fca-f904b5cf706d
73517-382-02	2025-01-30	C162847	48780-1	2cef2736-a2bd-d83d-e063-dadaa90ab31f	a93cd61a-ae83-4c45-8fca-f904b5cf706d
73517-382-03	2025-01-30	C162847	48780-1	2cef2736-a2bd-d83d-e063-dadaa90ab31f	a93cd61a-ae83-4c45-8fca-f904b5cf706d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73517-382-01	Pipette Mineral Sunscreen Broad SpectrumSPF50	120 mL in 1 TUBE	LOTION	120	5
73517-382-02	Pipette Mineral Sunscreen Broad SpectrumSPF50	30 mL in 1 TUBE	LOTION	30	5
73517-382-03	Pipette Mineral Sunscreen Broad SpectrumSPF50	15 mL in 1 TUBE	LOTION	15	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73517-382	PIPETTE MINERAL SUNSCREEN BROAD SPECTRUM SPF50 (ZINC OXIDE) LOTION [AMYRIS, INC]	5	Legacy NDC, 3 package rows	20221104_a93cd61a-ae83-4c45-8fca-f904b5cf706d.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 55 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CENTELLA SUNSCREEN Cream	ZINC OXIDE	Yunqi Cosmetics (Shenzhen) Co., Ltd	4cbac4e9-7540-f703-e063-6394a90ad808	2026-03-11	Warnings	Exact identifier application number: M020
Vacation Lip Balm	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Vacation INC.	4ba8ed52-2f52-40b9-a810-8450f9b90778	2026-03-10	Warnings	Exact identifier application number: M020
COOLA Zinc Oxide BodyLotion SPF 50 Fragrance-Free	ZINC OXIDE	COOLA LLC	4cad89a5-325c-b3c2-e063-6294a90ac225	2026-03-10	Warnings	Exact identifier application number: M020
Olay Complete plus Facial Moisturizer with Sunscreen Broad Spectrum SPF 40 Sensitive	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	4caf2ab5-76cb-4b0f-e063-6294a90a233e	2026-03-10	Warnings	Exact identifier application number: M020
EWC Slow Lightweight Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE	EWC Ventures, LLC	063426b8-d1cf-4ee2-8ab8-ff007227eab8	2026-03-10	Warnings	Exact identifier application number: M020
Olay Vitamin C Brightening Facial Moisturizer with Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	4cb268ea-f2b5-ddd1-e063-6394a90a1e96	2026-03-10	Warnings	Exact identifier application number: M020
Vacation Grand Cuvee Shimmer SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Vacation INC.	e0b3d90b-ba56-43e5-aa68-8e5f473628ff	2026-03-09	Warnings	Exact identifier application number: M020
La Roche Posay Laboratoire Dermatologique ANTHELIOS UVPRO SPORT INVISIBLE SUNSCREEN BROAD SPECTRUM SPF 45	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	L'Oreal USA, Inc.	77f46325-600c-40ff-94fc-ea82d43134c2	2026-03-09	Warnings	Exact identifier application number: M020
Civant 50 Sunscreen Broad Spectrum SPF 50	OCTOCRYLENE, ZINC OXIDE	Civant LLC	e23622b8-49dd-45b9-8c51-1a83181cc7bd	2026-03-09	Warnings	Exact identifier application number: M020
HydroScreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	METHODIQ INC.	4c9d5dfd-d790-fffc-e063-6294a90a4d30	2026-03-09	Warnings	Exact identifier application number: M020
Sunsei SPF 45 Sunscreen	ZINC OXIDE	Shimoda Prime Products, LLC	3d48e3e2-18c7-e004-e063-6294a90af4f2	2026-03-09	Warnings	Exact identifier application number: M020
Sunsei SPF 30 Sunscreen	ZINC OXIDE	Shimoda Prime Products, LLC	68df620b-7c1c-448c-93fd-91459e393c64	2026-03-09	Warnings	Exact identifier application number: M020
EADEM SUNSUEDE DAILY SUNSCREEN AND BLURRING PRIMER SPF50 PLUS	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	EADEM, Inc.	4ca05e2f-f0c5-821c-e063-6294a90a90b8	2026-03-09	Warnings	Exact identifier application number: M020
COOLA SunBlur Primer SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	COOLA LLC	4c6439e8-abda-663a-e063-6394a90ac43b	2026-03-06	Warnings	Exact identifier application number: M020
COOLA SunBlur Makeup Mist SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	COOLA LLC	4c666a82-293e-06df-e063-6294a90ad551	2026-03-06	Warnings	Exact identifier application number: M020
No 7 Restore and Renew Multi Action Fragrance Free Day Cream SPF 25	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	BCM Cosmetique SAS	4d6d1fda-da78-62ed-e063-6294a90ac105	2026-03-06	Warnings	Exact identifier application number: M020
Palio Sunscreen Broad Spectrum SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE	Sole Palio LLC	071d5113-8fe8-44bb-8322-542eafc2800a	2026-03-05	Warnings	Exact identifier application number: M020
Olay Age Defying Classic Broad Spectrum SPF 15	OCTINOXATE AND ZINC OXIDE	The Procter & Gamble Manufacturing Company	4c49dbf1-d1fe-ad4a-e063-6394a90af151	2026-03-05	Warnings	Exact identifier application number: M020
SPF 70 Kids Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Derma Care Research Labs, LLC	0aadc378-dc34-9a37-e063-6294a90ad49e	2026-03-05	Warnings	Exact identifier application number: M020
cle de peau BEAUTE RADIANT FLUID FOUNDATION NATURAL B50	OCTINOXATE AND TITANIUM DIOXIDE	SHISEIDO AMERICAS CORPORATION	4490f968-46b6-44d2-af2d-5130b52c8861	2026-03-05	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
73517-382-01	73517038201	120 mL in 1 TUBE (73517-382-01)	120 ml	2020-06-01	0000-00-00	No	No	Current
73517-382-02	73517038202	30 mL in 1 TUBE (73517-382-02)	30 ml	2020-06-01	0000-00-00	No	No	Current
73517-382-03	73517038203	15 mL in 1 TUBE (73517-382-03)	15 ml	2020-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Pipette Mineral Sunscreen Broad Spectrum SPF50 - Amyris, Inc	Amyris, Inc	2022-11-03	HUMAN OTC DRUG LABEL	5