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 113 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Tinted Mineral Sunscreen ZINC OXIDE WECARE FRISCO PLLC 37507b14-fc01-5e27-e063-6294a90afd50 2025-12-16 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen ZINC OXIDE WECARE FRISCO PLLC 375203a6-2ab8-2a80-e063-6294a90ada72 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen ZINC OXIDE WECARE FRISCO PLLC 3751caa3-867e-5901-e063-6294a90ab6bd 2025-12-16 Exact identifier application number: M020 Auset Tinted Replenishing Daily Protection ZINC OXIDE SHAYLA BOGER SKIN THERAPY LLC 37da48d6-8f12-ec97-e063-6294a90a699c 2025-12-16 Exact identifier application number: M020 Morning Replenish ZINC OXIDE KATHY JONES AESTHETHICS LLC 37da711e-840b-2f2a-e063-6294a90ab16c 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE KATHY JONES AESTHETHICS LLC 37dab729-5988-5eba-e063-6294a90ac6b7 2025-12-16 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Tory Sullivan, M.D., P.A. 36241e60-f02a-50a7-e063-6394a90a6390 2025-12-16 Exact identifier application number: M020 Ageless All Fitz ZINC OXIDE A.Wall Beauty LLC 37670cb1-ac75-5049-e063-6394a90a4d0a 2025-12-16 Exact identifier application number: M020 Tinted Replenishing Daily Protection ZINC OXIDE Tory Sullivan, M.D., P.A. 36244b27-20e5-f370-e063-6294a90a1f6c 2025-12-16 Exact identifier application number: M020 UV Defense Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC 365e09a8-308b-b753-e063-6394a90ae9e5 2025-12-16 Exact identifier application number: M020 UV Defense Mineral Sunscreen Tinted TITANIUM DIOXIDE, ZINC OXIDE CCLEAR SOLUTIONS ACNE & SKIN CARE CLINIC 365e2498-7df2-f22c-e063-6294a90ac6ab 2025-12-16 Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen non tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3bf5a6-33ec-0255-e063-6294a90ac96a 2025-12-16 Warnings Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3cba2e-acc6-a2df-e063-6294a90abf71 2025-12-16 Warnings Exact identifier application number: M020 Color Smart Tinted Mineral ZINC OXIDE MEGAN YORK INC. 365c4623-94d5-e8b6-e063-6394a90a966a 2025-12-16 Exact identifier application number: M020 Anti-Aging Tinted Sunscreen ZINC OXIDE KARINA SALDIVAR 3bca508e-7bd0-d45d-e063-6394a90a1730 2025-12-16 Warnings Exact identifier application number: M020 UV Protection Veil Mineral Sunscreen, tinted TITANIUM DIOXIDE, ZINC OXIDE ATHENA PLASTIC SURGERY 3b3c757f-6581-4978-e063-6294a90a6173 2025-12-16 Warnings Exact identifier application number: M020 Kind Restore Tinted Mineral Sunscreen ZINC OXIDE POLISH BEAUTY 3980810f-58b5-3a60-e063-6294a90a9c07 2025-12-16 Exact identifier application number: M020 Daydream Beyond Screen ZINC OXIDE ULTRAVIOLET SKINCARE LLC 36bfd963-d123-0d25-e063-6294a90aa827 2025-12-16 Exact identifier application number: M020 Virgo SOL Primer Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ULTRAVIOLET SKINCARE LLC 369d4f43-8c57-9fcf-e063-6294a90aa916 2025-12-16 Exact identifier application number: M020 Virgo SOL Non Tinted Mousse TITANIUM DIOXIDE, ZINC OXIDE ULTRAVIOLET SKINCARE LLC 369d63a9-b9ab-9530-e063-6394a90ac8ef 2025-12-16 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