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 44 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TRUST MD SPF30 STEM CELL FACE OCTINOXATE OCTISALATE HOMOSALATE AVOBENZONE TITANIUM DIOXIDE Guangzhou Yapheon Health Industry Co., Ltd. 4f2ca12c-bc6f-61b8-e063-6294a90a0d7e 2026-04-11 Warnings Exact identifier application number: M020 MIDHA Rice Daily Moisture Sun Cream AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE MIDHA Cosmetic Co.,Ltd. 4b394107-7830-c2c6-e063-6294a90a07d9 2026-04-10 Warnings Exact identifier application number: M020 Abib Dewy tinted sunscreen Glow tube Deep OCTISALATE, OCTOCRYLENE, ZINC OXIDE FOURCOMPANY CO., LTD. 4f15d5ba-6396-56bf-e063-6394a90adb06 2026-04-10 Warnings Exact identifier application number: M020 Abib Dewy tinted sunscreen Glow tube Light OCTISALATE, OCTOCRYLENE, ZINC OXIDE FOURCOMPANY CO., LTD. 4f165895-aa84-e215-e063-6394a90a6256 2026-04-10 Warnings Exact identifier application number: M020 Abib Dewy tinted sunscreen Glow tube Medium OCTISALATE, OCTOCRYLENE, ZINC OXIDE FOURCOMPANY CO., LTD. 4f16b8a4-4279-5f79-e063-6294a90a353d 2026-04-10 Warnings Exact identifier application number: M020 Sheer Touch Sunscreen SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE Amazon.com Services LLC f5ca0416-548c-4be0-a69e-c7e1b52aba95 2026-04-10 Warnings, Adverse reactions Exact identifier application number: M020 LASPA TINTED MATTE SUNSCREEN SPF 20 LIGHT ZINC OXIDE The Green Cricket Inc c56fd135-f46a-51ce-e053-2a95a90ab7b3 2026-04-10 Warnings Exact identifier application number: M020 CorTex SunX 50 Thick AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CoreTex Products Inc f67a6c6c-c314-1c9d-e053-2a95a90a7f1a 2026-04-10 Warnings Exact identifier application number: M020 Nu Skin 180 Degree UV Block Hydrator SPF 18 OCTINOXATE AND ZINC OXIDE NSE Products, Inc. b9635e59-bb08-4167-b7ba-54c3fc712589 2026-04-09 Warnings Exact identifier application number: M020 Sport Sunscreen SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE The Kroger Co. 79c6fe2a-34c2-44cc-81bc-796c4463d2a6 2026-04-09 Warnings, Adverse reactions Exact identifier application number: M020 Arizona Sun ProductsSurfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fdbae5-84ec-7b1d-e063-6294a90a2878 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Prickly Pear Lip Balm SPF 15 SUNSCREEN LIP BALM Arizona Sun Products 11e9cb25-6ff8-a121-e063-6394a90a849e 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen SPF 8 SUNSCREEN Arizona Sun Products 11e8b612-29be-47ed-e063-6394a90ab9e7 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun ProductsSurfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fdcfd0-8b24-7efc-e063-6294a90af7fa 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Cycleblok Sunscreen SUNSCREEN Arizona Sun Products 11e71a84-12d1-2d4f-e063-6294a90adcd6 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Bikerblok Sunscreen SUNSCREEN Arizona Sun Products 11e6eafd-f967-b748-e063-6394a90aabfd 2026-04-09 Warnings Exact identifier application number: M020 YSE Beauty Skin Glow Primer SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE MSS Beauty LLC 6a318e27-14e5-488e-ac19-010f69cb743d 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen Kids Water Resistant SPF 30 SUNSCREEN Arizona Sun Products 116ed17c-3b38-5e96-e063-6294a90a4246 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Surfblok Sunscreen SUNSCREEN Arizona Sun Products 11e76815-9316-555d-e063-6294a90aeb81 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Moisturizer SPF 3 MOISTURIZER Arizona Sun Products 1171af26-3040-552c-e063-6294a90ae220 2026-04-09 Warnings 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