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 16 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Daily Wear Face Protection Mineral Based Sunscreen SPF 16 - Fair Light ZINC OXIDE REJUVA MINERALS INC 2abccc86-01d4-e45c-e063-6294a90a7f8b 2026-07-02 Warnings Exact identifier application number: M020 OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige TITANIUM DIOXIDE LG H&H Co., Ltd. d307471c-6cc6-ce48-e053-2995a90a3e02 2026-07-02 Warnings Exact identifier application number: M020 Sunscreen SPF 50 AVOBENZONE 3% HOMOSALATE 10% OCTOCRYLENE 5% Worthy Promotional Products f5e2a412-e891-411d-85da-89f38cd61a9b 2026-07-02 Warnings Exact identifier application number: M020 Bath and Body Works SPF Bronze Kiss AVOBENZONE,HOMOSALATE,OCTISALATE Bath & Body Works, Inc. 5606c57b-7fdb-4317-e063-6294a90a996c 2026-07-02 Warnings Exact identifier application number: M020 Evereden Kids Mineral Sunscreen SPF 30 ZINC OXIDE Eden Brands Inc bba219a4-de83-76fd-e053-2995a90a2d69 2026-07-01 Warnings Exact identifier application number: M020 Kids Mineral Face Cream SPF20 ZINC OXIDE Eden Brands Inc fbfccb0c-e459-3282-e053-6394a90ad95d 2026-07-01 Warnings Exact identifier application number: M020 Evereden Fluid Silk Mineral Sunscreen PRO SPF50 TITANIUM DIOXIDE, ZINC OXIDE Eden Brands Inc. 2cb7773f-9a05-ad02-e063-6294a90af024 2026-07-01 Warnings Exact identifier application number: M020 Zinc Oxide 20% SUNSCREEN SPF 50 The Beach Rooster c2e57236-f184-4fa8-8fd5-c44cbf230058 2026-07-01 Warnings Exact identifier application number: M020 ISNTREE HYALURONIC ACID WATERY SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE ISNTREE Inc. 557477a2-def8-740b-e063-6294a90ad287 2026-06-30 Warnings Exact identifier application number: M020 HealthyDerm tallow mineral sunscreen SPF50 ZINC OXIDE 25% VIRENTIA LLC 557b0b1f-8cd9-735a-e063-6294a90ad60e 2026-06-30 Warnings Exact identifier application number: M020 OHUI Ultimate Cover CC Cushion Compact 01 Light Beige TITANIUM DIOXIDE LG H&H Co., Ltd. d2f9c54b-ac4e-5141-e053-2a95a90aa2b8 2026-06-30 Warnings Exact identifier application number: M020 Christian Dior Invisible UV Stick Broad Spectrum SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Parfums Christian Dior 8e3840b2-b404-474f-aff7-dec3a64a70a4 2026-06-29 Warnings Exact identifier application number: M020 TOCOBO Blur Finish Sun Cushion Cotton Blue HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE PICTON Co., Ltd. 4d6ddee3-9a76-6c9c-e063-6394a90a1529 2026-06-29 Warnings Exact identifier application number: M020 Sun Bum Coconut Lip 30 Sunscreen Lip Balm AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Sun Bum, LLC 20d942fa-93de-45a8-e063-6294a90a2b49 2026-06-29 Warnings Exact identifier application number: M020 AVON ANEW SOLAIRE EVERYDAY MINERAL FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN ZINC OXIDE THE AVON COMPANY 54f7c1d1-acdb-fd25-e063-6294a90a8173 2026-06-29 Warnings Exact identifier application number: M020 Earth Baby Broad Spectrum SPF 30 SUNSCREEN Earth Baby, Inc. 42556876-74ea-38e6-e054-00144ff8d46c 2026-06-28 Warnings Exact identifier application number: M020 TOCOBO Cotton Airy Sun Stick AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE PICTON CO., Ltd. 55364026-c55a-b370-e063-6294a90ae0d1 2026-06-27 Warnings Exact identifier application number: M020 Sun Does Matter Daily Face Sunscreen HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE Sundoesmatter Company Inc. 553687d8-d4e1-8361-e063-6294a90a24fe 2026-06-27 Warnings Exact identifier application number: M020 ORLASKIN HYDRATING SUNSCREEN SPF 50 OCTOCRYLENE ETHYLHEXYL METHOXYCINNAMATE ETHYLHEXYL SALICYLATE AVOBENZONE Guangzhou Yapheon Health Industry Co., Ltd. 552b4c87-4621-d5a7-e063-6294a90a042e 2026-06-26 Warnings Exact identifier application number: M020 Bath and Body Works SPF Waikiki Beach Coconut AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE Bath & Body Works, Inc. 1c30de8a-4d29-bbac-e063-6294a90a84d9 2026-06-26 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