Home NDC 72104-062 Truffoire Truffle Brightening
Product NDC 72104-062
11-digit product format 721040062
Labeler code 72104
Product ID 72104-062_1a76e5ea-11b0-477e-ab46-c6ad68e11abb
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Homosalate, Octisalate, Oxybenzone and Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler Innovation Brands Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-07-27
Substance OCTINOXATE; HOMOSALATE; OCTISALATE; OXYBENZONE; AVOBENZONE
Active strength 7.4; 6.2; 5.2; 3.1; 1.5 g/100g; g/100g; g/100g; g/100g; 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 · 14 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 2025-04-01 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 72104-062-84 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 72104-062-84 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 72104-062-84 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 72104-062-84 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 72104-062-84 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 72104-062-84 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 72104-062-84 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Truffoire Truffle Brightening
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.4 g/100g HOMOSALATE 6.2 g/100g OCTISALATE 5.2 g/100g OXYBENZONE 3.1 g/100g AVOBENZONE 1.5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72104-062-84 Truffoire Truffle Brightening 1 in 1 CARTON CREAM 1 3 72104-062-84 Truffoire Truffle Brightening 50 g in 1 JAR CREAM 50 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72104-062 TRUFFOIRE TRUFFLE BRIGHTENING (OCTINOXATE, HOMOSALATE, OCTISALATE, OXYBENZONE AND AVOBENZONE) CREAM [LIONESSE USA, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20220819_e3068ecf-0bee-4e8a-a439-4bb707a2845d.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 5 of 361 · 7,213 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hawaiian Tropic AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE Edgewell Personal Care Brands LLC 5991466a-e729-16b7-e063-6394a90a11ff 2026-08-21 Warnings Exact identifier application number: M020 Avobenzone, Homosalate, Octisalate AVOBENZONE, HOMOSALATE, OCTISALATE Topco Associates LLC 597b78df-83cb-1b21-e063-6294a90a56a8 2026-08-20 Warnings, Adverse reactions Exact identifier application number: M020 Sunski Base Camp Face and Body Sunscreen SPF 45 HOMOSALATE, OCTISALATE, AVOBENZONE Stewart Charley Ventures, LLC 2fc45f85-a6f8-4893-8b34-4db5e39cb615 2026-08-20 Warnings Exact identifier application number: M020 Sweat Resistant Sunscreen Body Original TITANIUM DIOXIDE, ZINC OXIDE Clutch, Inc. 4bbde755-e312-123e-e063-6294a90a467f 2026-08-20 Warnings Exact identifier application number: M020 Sunscreen BROAD SPECTRUM SPF 30 Concierge Choice LLC 5980055b-493e-4763-e063-6294a90a570f 2026-08-20 Warnings Exact identifier application number: M020 Lip Balm SPF 15 AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE Skin Script, LLC 20c5fde7-ee8f-4b74-e063-6394a90a93ec 2026-08-19 Warnings Exact identifier application number: M020 Aloe UP .5OZ SPF 50 MINERAL Sunscreen ZINC OXIDE 14.69% Aloe Care International, LLC 6ad80af3-78cd-4211-a5f2-68531aae264a 2026-08-19 Warnings Exact identifier application number: M020 Utu Broad Spectrum SPF 50 Tinted Sunscreen-Stick ZINC OXIDE Utu Co 596e17d3-3064-1cda-e063-6294a90af963 2026-08-19 Warnings Exact identifier application number: M020 Mineral sunscreen MINERAL SUNSCREEN Guangzhou Origin Beauty Cosmetics Co., Ltd. 59713657-a7ef-1aee-e063-6394a90a326e 2026-08-19 Warnings Exact identifier application number: M020 The Naked Bee SPF 50 Mineral Sunscreen ZINC OXIDE 14.69% The Naked Bee f820a9be-c94d-4fd5-b202-2dda5746a82a 2026-08-18 Warnings Exact identifier application number: M020 The Naked Bee SPF 50 Mineral Sunscreen ZINC OXIDE 20% The Naked Bee 7dd2b1cd-e229-4eeb-8122-46fde5af1091 2026-08-18 Warnings Exact identifier application number: M020 Sun Zapper - Baby pure zinc sunscreen SPF30 ZINC OXIDE SUNSCREEN VEGANIC SKN LIMITED 3ee52faa-64a8-4bdf-e063-6294a90a65cf 2026-08-17 Warnings Exact identifier application number: M020 Sun Zapper - Face pure zinc sunscreen SPF30 ZINC OXIDE SUNSCREEN VEGANIC SKN LIMITED 3ee4feb3-6966-67f9-e063-6394a90a16d5 2026-08-17 Warnings Exact identifier application number: M020 HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN ZINC OXIDE,TITANIUM DIOXIDE Guangzhou Tata Biotechnology Co., Ltd. 4339df13-77d3-31a1-e063-6394a90a5208 2026-08-17 Warnings Exact identifier application number: M020 Soleil Defense Sunscreen BROAD SPECTRUM SPF 30 AMARA MED SPA LLC 594244b1-db3b-002b-e063-6394a90a0329 2026-08-17 Warnings Exact identifier application number: M020 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 HAMBLIN DERMATOLOGY 5942e64c-416e-7525-e063-6394a90a2839 2026-08-17 Warnings Exact identifier application number: M020 Protect Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 Opal Day Spa 5943413a-48e1-0bdf-e063-6294a90a2fff 2026-08-17 Warnings Exact identifier application number: M020 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 MedSpa By Beauty Bar LLC 5943ba3d-688e-9e9c-e063-6294a90afa9a 2026-08-17 Warnings Exact identifier application number: M020 Sunscreen BROAD SPECTRUM SPF 30 Charleston Dermatology, P.C. 59440f7f-4213-6e2b-e063-6394a90af483 2026-08-17 Warnings Exact identifier application number: M020 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 CORBY, JR., TERRY L. 594443fd-8e27-4ec6-e063-6294a90a3ff0 2026-08-17 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 72104-062-84 72104006284 1 JAR in 1 CARTON (72104-062-84) / 50 g in 1 JAR 1 jar 2021-07-27 0000-00-00 No No Current