Home NDC 73517-382 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 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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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 128 of 353 · 7,041 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Sheer Sunscreen ZINC OXIDE SKINBAR MD LLC 35810a90-e2ca-b80b-e063-6294a90a14f0 2025-12-12 Exact identifier application number: M020 Tinted Facial Mineral Sunscreen SPF 40 TITANIUM DIOXIDE, ZINC OXIDE RSL89 LLC 3531d609-a0d8-cb59-e063-6394a90a4bea 2025-12-12 Exact identifier application number: M020 Non-Tinted Zinc Body And Face SPF40 ZINC OXIDE RSL89 LLC 3532102c-8ded-1e78-e063-6294a90ae224 2025-12-12 Exact identifier application number: M020 Non-Tinted Zinc Body And Face SPF40 ZINC OXIDE RSL89 LLC 35330a82-dc6b-49af-e063-6394a90af9ea 2025-12-12 Exact identifier application number: M020 Tinted Replenishing SPF40 ZINC OXIDE RSL89 LLC 353257db-6c30-4a03-e063-6294a90ae45d 2025-12-12 Exact identifier application number: M020 Tinted Facial Mineral Sunscreen SPF 40 TITANIUM DIOXIDE, ZINC OXIDE RSL89 LLC 3532a6a2-dbb5-8111-e063-6294a90aeaeb 2025-12-12 Exact identifier application number: M020 Tinted Replenishing SPF40 ZINC OXIDE RSL89 LLC 35334c75-b3fd-37fa-e063-6294a90ab3b0 2025-12-12 Exact identifier application number: M020 Age Defying Sunscreen ZINC OXIDE GINAMARIE Products 35835565-f10b-e8e7-e063-6394a90ab2d3 2025-12-12 Exact identifier application number: M020 Tinted Daily Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE RSL89 LLC 35338026-525a-d8b3-e063-6394a90a98f5 2025-12-12 Exact identifier application number: M020 Mineral Lip Protection TITANIUM DIOXIDE, ZINC OXIDE RSL89 LLC 3541971e-3664-a9f5-e063-6294a90ac2d2 2025-12-12 Exact identifier application number: M020 Age Defying Sunscreen ZINC OXIDE GINAMARIE Products 35837cf7-91e5-f9ec-e063-6394a90aa91e 2025-12-12 Exact identifier application number: M020 Mineral Sunscreen Face plus Body ZINC OXIDE KS Esthetics, LLC 390a4d8d-b47f-0d9a-e063-6394a90a9b53 2025-12-12 Exact identifier application number: M020 Mineral Sunscreen Tinted Zinc Oxide ZINC OXIDE KS Esthetics, LLC 3909e657-97a5-dd3c-e063-6394a90a10eb 2025-12-12 Exact identifier application number: M020 Prime Protection Sunscreen non tinted TITANIUM DIOXIDE, ZINC OXIDE KRISTI REDD ESTHETICS 36608832-22d8-bc76-e063-6394a90abac6 2025-12-12 Exact identifier application number: M020 Prime Protection Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE KRISTI REDD ESTHETICS 3660af9e-d60f-c33e-e063-6394a90a3a05 2025-12-12 Exact identifier application number: M020 Hydrating Antioxidant Sunscreen tinted ZINC OXIDE KRISTI REDD ESTHETICS 366149e2-b03c-e798-e063-6394a90a6a1d 2025-12-12 Exact identifier application number: M020 Prime Protection Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE KRISTI REDD ESTHETICS 3660e701-1373-eef4-e063-6394a90a6140 2025-12-12 Exact identifier application number: M020 Hydrating Antioxidant Sunscreen tinted ZINC OXIDE KRISTI REDD ESTHETICS 3661251d-b907-8df6-e063-6294a90a1c73 2025-12-12 Exact identifier application number: M020 sheer tinted sunscreen TITANIUM DIOXIDE, ZINC OXIDE SARA ELIZABETH SKINCARE 3b177c49-ed8c-42b9-e063-6294a90a82c6 2025-12-12 Warnings Exact identifier application number: M020 Canopy Untinted ZINC OXIDE BORREGO SPRINGS SKINCARE LLC 35824cd5-0036-7886-e063-6394a90ae678 2025-12-12 Exact identifier application number: M020
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