Home NDC 44099-011 skin MD
Product NDC 44099-011
11-digit product format 440990011
Labeler code 44099
Product ID 44099-011_4384c3d1-e160-67fa-e063-6394a90a0a42
Type HUMAN OTC DRUG
Nonproprietary name octinoxate, octisalate, homosalate
Dosage form LOTION
Route TOPICAL
Labeler 21st Century Formulations
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-08-19
Substance OCTINOXATE; OCTISALATE; HOMOSALATE
Active strength 7; 5; 3 mg/100mL; mg/100mL; mg/100mL
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 · 15 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 package package 44099-011-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 44099-011-04 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 44099-011-03 D Discontinued by firm d630ba8d3edf…732f749b63fb…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 44099-011-04 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 44099-011-03 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 44099-011-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 44099-011-05 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 44099-011-01 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 44099-011-04 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 44099-011-03 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 44099-011-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 44099-011-05 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 44099-011-01 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 skin MD
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7 mg/100mL OCTISALATE 5 mg/100mL HOMOSALATE 3 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W Internal UNII lookup V06SV4M95S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44099-011-01 skin MD 117 mL in 1 BOTTLE LOTION 117 7 44099-011-02 skin MD 236 mL in 1 BOTTLE LOTION 236 7 44099-011-03 skin MD 3785 mL in 1 BOTTLE LOTION 3785 7 44099-011-04 skin MD 100 mL in 1 TUBE LOTION 100 7 44099-011-05 skin MD 200 mL in 1 TUBE LOTION 200 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44099-011 SKIN MD (OCTINOXATE, OCTISALATE, HOMOSALATE) LOTION [21ST CENTURY FORMULATIONS] 6 Current NDC, Legacy NDC, 5 package rows 20250406_e809e1d3-0a6d-730d-e053-2a95a90aedb9.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 49 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join MENOKIN 30 SECONDS GLOW AND CLEAR Gel SUNSCREEN BRIGHT AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Forest Avenue Co., Ltd. 8de4ec46-f60a-4c51-a16e-9140150e2162 2026-04-01 Warnings Exact identifier application number: M020 ChapStick Moisturizer Cool Mint SPF 15 SPF 15 LIP PROTECTANT Suave Brands Co., LLC 42f50497-ded1-6863-e063-6294a90a39c8 2026-03-31 Warnings Exact identifier application number: M020 Purito Sunday Adventure Sunscreen SPF 50, 50 mL AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Hinature bf16f535-97fc-4fd8-9310-8b6bbc82baae 2026-03-31 Warnings Exact identifier application number: M020 spf 50 mineral powder sunscreen TITANIUM DIOXIDE, ZINC OXIDE Smalls Brand LLC DBA Roe Wellness f8762dd1-0484-74ea-e053-6294a90ac112 2026-03-31 Warnings Exact identifier application number: M020 Badger SPF 30 Face Mineral Sunscreen ZINC OXIDE W.S. Badger Company, Inc. 14a9b605-f1f0-00e5-e063-6394a90a5a51 2026-03-31 Warnings Exact identifier application number: M020 Covergirl cgsmoothers BB Tinted Moisturizer Broad Spectrum SPF 21 (all shades) OCTINOXATE AND ZINC OXIDE Noxell Corporation 38bba282-b4f7-4374-8732-419400b1cc50 2026-03-31 Warnings Exact identifier application number: M020 SeranovaTM ULTRALIGHT SPF50 SERUM SERANOVATM ULTRALIGHT SPF50 SERUM Guangzhou Ariel Biotech Co., Ltd. 4e5d716d-2b2d-d42f-e063-6294a90a1e52 2026-03-31 Warnings Exact identifier application number: M020 ageLOC Tru Face Radiant Day AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE NSE Products, Inc. 3e9a0b39-4351-41df-81b2-88c1c15c0db2 2026-03-31 Warnings Exact identifier application number: M020 Sunright Solar Screen Mineral Face Sunscreen ZINC OXIDE NSE Products, Inc. 93a32040-3a47-4d6f-baa1-5a4595bef410 2026-03-31 Warnings Exact identifier application number: M020 Lancome Paris Renergie HPN 300 Peptide Sunscreen Broad Spectrum SPF 25 High-Performance Day AVOBENZONE, OCTISALATE, AND OCTOCRYLENE L'Oreal USA Products Inc 28f500e2-41d1-4747-8f26-3f6f8cc1b583 2026-03-30 Warnings Exact identifier application number: M020 Lancome Paris Renergie HPN 300 Peptide Sunscreen Broad Spectrum SPF 25 High-Performance Day AVOBENZONE, OCTISALATE, AND OCTOCRYLENE SICOS ET CIE dd448b7a-2554-4dfc-9eb3-ec3486ec6197 2026-03-30 Warnings Exact identifier application number: M020 ANUA MINERAL WEIGHTLESS FINISH SUNSCREEN ZINC OXIDE Thefounders 4e37d291-84fb-252a-e063-6294a90acd1f 2026-03-30 Warnings Exact identifier application number: M020 Beyond Glow Tinted Mineral Sunscreen Broad Spectrum SPF 50 ZINC OXIDE THE AVON COMPANY 4e43bea2-247d-fe11-e063-6294a90a33a3 2026-03-30 Warnings Exact identifier application number: M020 Abib Quick sunstick Protection bar HOMOSALATE,OCTOCRYLENE,OCTISALATE,AVOBENZONE FOURCOMPANY CO., LTD. 1a2ab632-643f-1aa9-e063-6394a90a0c05 2026-03-30 Warnings Exact identifier application number: M020 ChapStick Classic Original Military SKIN PROTECTANT LIP BALM Suave Brands Co., LLC 4514490b-f348-4526-e063-6294a90ad505 2026-03-30 Warnings Exact identifier application number: M020 ChapStick Moisturizer Black Cherry SPF 15 SPF 15 SKIN PROTECTANT Suave Brands Co., LLC 42f40978-51ca-f448-e063-6294a90acf31 2026-03-30 Warnings Exact identifier application number: M020 Sky and Sol Face and Body Sunscreen SPF 50 NON- NANO ZINC OXIDE Delta Ecommerce LLC 473a6ade-1f0a-c711-e063-6294a90a2b83 2026-03-30 Warnings Exact identifier application number: M020 Vacation by Vacation Scent and Shimmer Duo AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE Vacation Inc. 0c4e6fa1-c78d-4f9d-969f-135d4ed67daf 2026-03-30 Warnings Exact identifier application number: M020 Marie originals - ProActive Sunscreen ZINC OXIDE SUNSCREEN VEGANIC SKN LIMITED 4e3204bf-eda4-2bdf-e063-6394a90ae429 2026-03-29 Warnings Exact identifier application number: M020 Sport Ultra AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CARDINAL HEALTH 110, LLC. DBA LEADER 37c5dcf7-dc2d-624f-e063-6394a90ae992 2026-03-29 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 44099-011-01 44099001101 117 mL in 1 BOTTLE (44099-011-01) 117 ml 2008-08-19 0000-00-00 No No Current 44099-011-02 44099001102 236 mL in 1 BOTTLE (44099-011-02) 236 ml 2008-08-19 0000-00-00 No No Current 44099-011-03 44099001103 3785 mL in 1 BOTTLE (44099-011-03) 3785 ml 2008-08-19 0000-00-00 No No Current 44099-011-04 44099001104 100 mL in 1 TUBE (44099-011-04) 100 ml 2018-07-16 0000-00-00 No No Current 44099-011-05 44099001105 200 mL in 1 TUBE (44099-011-05) 200 ml 2018-07-16 0000-00-00 No No Current