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 47 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Neutrogena Ultra Gentle Daily Facial Moisturizer Sunscreen Broad Spectrum SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Acupac Packaging, Inc. 4ef669b9-df00-8965-e063-6394a90ab335 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena Collagen Bank SPF Moisturizer Sunscreen Broad Spectrum SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Acupac Packaging, Inc. 4ef6a60a-6634-e79b-e063-6394a90a3daa 2026-04-08 Warnings Exact identifier application number: M020 Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc. 4ef6b5fb-5495-001c-e063-6394a90ab7b3 2026-04-08 Warnings Exact identifier application number: M020 Sunright Lip Balm OCTINOXATE, AVOBENZONE, AND OCTOCRYLENE NSE Products, Inc. dfdb2d0a-c646-4c44-b648-e2fdd604cdc9 2026-04-08 Warnings Exact identifier application number: M020 Nu Colour Bioadaptive BB Plus Foundation - Light Golden TITANIUM DIOXIDE NSE Products, Inc. faae6f47-19f3-41cb-8e0d-388569b5c73d 2026-04-07 Warnings Exact identifier application number: M020 Ultra Sunscreen OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE Jiangsu Senwo Medical Technology Co., Ltd. 4ed974b8-6c11-08e0-e063-6294a90a7713 2026-04-07 Warnings Exact identifier application number: M020 Vivaiodays SPF 30 Sunscreen with Turmeric SPF 30 SUNSCREEN WITH TURMERIC 5SENCO INC 4ee0c93a-7f50-2bda-e063-6294a90abff4 2026-04-07 Warnings Exact identifier application number: M020 Neutrogena MINERAL UV TINT FACE MEDIUM DEEP SPF 30 TITANIUM DIOXIDE, ZINC OXIDE Acupac Packaging, Inc 4ee39bbf-b7d7-8f87-e063-6294a90a2539 2026-04-07 Warnings Exact identifier application number: M020 BEVERLY HILLS MD SHEER RADIANCE SPF DROPS SUNSCREEN ZINC OXIDE Beverly Hills MD, LLC 4ed34743-cc68-501b-e063-6294a90ad396 2026-04-07 Warnings Exact identifier application number: M020 Nu Colour Bioadaptive BB plus Foundation - Beige TITANIUM DIOXIDE NSE Products, Inc. f74e83fe-41a0-4998-ae53-30ed5af47592 2026-04-07 Warnings Exact identifier application number: M020 Thinksport SPF 30 ZINC OXIDE thinkOperations,LLC 33065919-9b4e-4b2b-9306-a706558241c8 2026-04-07 Warnings Exact identifier application number: M020 Nutricentials Day Dream Protective HOMOSALATE, OCTISALATE, AVOBENZONE, AND OCTOCRYLENE NSE Products, Inc daca8347-f7e7-4733-bd22-1da7a6076fad 2026-04-06 Warnings Exact identifier application number: M020 TONEfitSUN Ultra Moisturizing Vegan Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory 4ec58c23-16b1-03bb-e063-6394a90a46c0 2026-04-06 Warnings Exact identifier application number: M020 Dior Forever Velvet Veil 24H Mattifying Makeup Base Blurring-Smoothing Pore Refining Effect with Sunscreen SPF 15 HOMOSALATE, OCTISALATE, OCTOCRYLENE Parfums Christian Dior be36b83f-662d-49c6-a12f-a64e11721d0c 2026-04-06 Warnings Exact identifier application number: M020 Pure Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Liz Corporation Ltd 4eca5257-6840-2a33-e063-6394a90ade28 2026-04-06 Warnings Exact identifier application number: M020 Dior Forever Skin Veil 24H Glow Hydrating Base Plumping and Smoothing Effect Hyaluronic Acid with Sunscreen SPF 25 ENSULIZOLE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Parfums Christian Dior 4a5147f3-4e52-447a-a89c-058aea8a612c 2026-04-06 Warnings Exact identifier application number: M020 Simple Mineral Sunscreen SPF 50 ZINC OXIDE Simple Sunscreen LLC c38cb4fa-8b8d-4c2d-9c32-301e120db1a1 2026-04-06 Warnings Exact identifier application number: M020 Badger SPF 50 Adventure Sport Mineral Sunscreen Cream ZINC OXIDE W.S. Badger Company, Inc. 2a96c423-f4ad-0f07-e063-6394a90a39f8 2026-04-06 Warnings Exact identifier application number: M020 Sheer Touch Sunscreen SPF 55 AVOBENZONE, HOMOSALATE, OCTISALATE Amazon.com Services LLC 03fce792-bcbb-4848-bc87-8913ecbe0786 2026-04-06 Warnings, Adverse reactions Exact identifier application number: M020 Sport Sunscreen SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE Amazon.com Services LLC 8937705d-b745-4b8c-bf9b-89e64a1e52b1 2026-04-06 Warnings, Adverse reactions 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