Home NDC 79753-012 Liplux
Product NDC 79753-012
11-digit product format 797530012
Labeler code 79753
Product ID 79753-012_2e57ccfc-f187-4dbe-e063-6394a90a2019
Type HUMAN OTC DRUG
Nonproprietary name Classic
Dosage form STICK
Route TOPICAL
Labeler COOLA LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 5; 8; 3 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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 79753-012-01 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 79753-012-01 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 79753-012-01 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 79753-012-01 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 79753-012-01 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 79753-012-01 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 79753-012-01 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 79753-012-01 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 79753-012-01 1332a3947898…d4bfe170f9cd…
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 Liplux
Brand name suffix SPF 30 Lip Balm
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 5 g/100g OCTOCRYLENE 8 g/100g AVOBENZONE 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup G63QQF2NOX Internal UNII lookup
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 79753-012-01 LipluxSPF 30 Lip Balm 4.2 g in 1 TUBE STICK 4.2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79753-012 LIPLUX SPF 30 LIP BALM (CLASSIC) STICK [COOLA LLC] 2 Current NDC, Legacy NDC, 1 package rows 20250223_b47b5f3a-43f3-ae7a-e053-2995a90ae16d.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 118 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Non Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 39959db9-5ee1-a27c-e063-6394a90a1e10 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen Stick TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3995f556-20fe-3e64-e063-6294a90a5efe 2025-12-15 Exact identifier application number: M020 Mineral Lip Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3995385b-b10b-ca5c-e063-6294a90af43f 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 3994aa84-30b4-3dc4-e063-6394a90a23e7 2025-12-15 Exact identifier application number: M020 Non Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE MILESTHETICS LLC 39947913-f1cc-25d2-e063-6294a90a4229 2025-12-15 Exact identifier application number: M020 Non Tinted Mineral Sunscreen ZINC OXIDE Micro Fibro Blast 35425e24-3e2c-51db-e063-6394a90a5580 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted ZINC OXIDE DENISE BELL SKIN CARE 396fe2ca-eb29-5952-e063-6294a90ab279 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f91b3-3326-3239-e063-6294a90a5df9 2025-12-15 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE Micro Fibro Blast 35422370-eb55-049c-e063-6294a90ad0a4 2025-12-15 Exact identifier application number: M020 Eclipse Face Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f0151-2d0d-f4da-e063-6394a90a5f7f 2025-12-15 Exact identifier application number: M020 Eclipse Body Non Tinted ZINC OXIDE DENISE BELL SKIN CARE 396f56df-d0de-1344-e063-6294a90a46ea 2025-12-15 Exact identifier application number: M020 Solar Shield Tinted TITANIUM DIOXIDE, ZINC OXIDE DENISE BELL SKIN CARE 396eb781-5947-3665-e063-6294a90a38dd 2025-12-15 Exact identifier application number: M020 Sun Veil Illuminating Sunscreen SPF30 ZINC OXIDE Koco Life LLC 46001097-540e-65da-e063-6294a90af299 2025-12-15 Warnings Exact identifier application number: M020 Mineral Primer tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 3542d8d3-35a3-7d63-e063-6394a90a6fd1 2025-12-15 Exact identifier application number: M020 Mineral Primer non-tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 354357de-1a85-3bdb-e063-6294a90aa9a2 2025-12-15 Exact identifier application number: M020 Mineral Primer tinted SPF40 TITANIUM DIOXIDE, ZINC OXIDE Oracle Esthetics, LLC 35433254-1dc8-a8f3-e063-6394a90a29f0 2025-12-15 Exact identifier application number: M020 Sun Therapy Sunscreen ZINC OXIDE Skin Therapy Studio LLC 3544916b-3f63-3a7a-e063-6394a90ae507 2025-12-15 Exact identifier application number: M020 Ultra Zinc Mineral Non Tinted ZINC OXIDE Skin Therapy Studio LLC 3545d603-3d01-c51d-e063-6394a90a1599 2025-12-15 Exact identifier application number: M020 Sun Therapy Sunscreen ZINC OXIDE Skin Therapy Studio LLC 357efafb-aa1c-0d69-e063-6394a90a5135 2025-12-15 Exact identifier application number: M020 Ultra Zinc Mineral Non Tinted ZINC OXIDE Skin Therapy Studio LLC 35806102-6919-116f-e063-6294a90ad922 2025-12-15 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 79753-012-01 79753001201 4.2 g in 1 TUBE (79753-012-01) 4.2 g 2020-01-01 0000-00-00 No No Current