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 31 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SunPlus Healthy Skin Sunny Living SPF 30 Mist Sunscreen AVOBENZONE, OCTISALATE, OCTOCRYLENE SUNPLUS SKIN CARE LLC 9b168046-3536-4ba9-9b5f-4f8c50b8b354 2026-05-14 Warnings Exact identifier application number: M020 SunPlus Healthy Skin Sunny Living SPF 50 Mist Sunscreen AVOBENZONE, OCTISALATE, OCTOCRYLENE SUNPLUS SKIN CARE LLC 0e60ecee-d9f4-47e0-92f7-ff319e4422dd 2026-05-14 Warnings Exact identifier application number: M020 Hampton Sun SPF 15 Sunscreen OCTOCRYLENE 7.50% AVOBENZONE 2.50% OCTISALATE 5.00% S&C Hampton Sun LLC 3ce75e74-b5d3-4fbe-8d44-9b6f14f354df 2026-05-14 Warnings Exact identifier application number: M020 Target Up and Up SPF 30 Deep Repair Facial Moisturizer Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE TARGET CORPORATION 51c9bdee-dcff-2818-e063-6294a90abb47 2026-05-14 Warnings Exact identifier application number: M020 Hampton Sun SPF 50 Baby Mineral ZINC OXIDE 20% S&C Hampton Sun LLC 42037d8c-4787-4e16-93fe-0d19b6b888fd 2026-05-14 Warnings Exact identifier application number: M020 Lancome Paris Renergie Lift MultiAction Sunscreen Broad Spectrum SPF 15 Firming AntiWrinkle AVOBENZONE, OCTISALATE AND OCTOCRYLENE SICOS ET CIE 29c9d1cb-e249-47fa-a46d-42190e59d352 2026-05-14 Warnings Exact identifier application number: M020 Hampton SPF 15 UV-Advanced Sunscreen HOMOSALATE 7.50% OCTISALATE 5.00% AVOBENZONE 3.00% S&C Hampton Sun LLC 1659a681-6cf8-45ba-b1f8-e330eee3b9d4 2026-05-14 Warnings Exact identifier application number: M020 Easy Everything Sunscreen ZINC OXIDE VLT Ventures LLC 51cd48cf-38ae-f347-e063-6294a90a8a90 2026-05-14 Warnings Exact identifier application number: M020 Hampton Sun SPF 4 OCTOCRYLENE 4.00% AVOBENZONE 2.00% S&C Hampton Sun LLC 68763abc-0d6b-441c-9a99-cf3dc86e6deb 2026-05-14 Warnings Exact identifier application number: M020 Easy Everything Sunscreen ZINC OXIDE VLT Ventures LLC 51cdbac3-7f44-d72d-e063-6294a90a2f99 2026-05-14 Warnings Exact identifier application number: M020 Round Lab x OUWR Birch Juice Moisturizing UVLOCK Gift Set AVOBENZONE, HOMOSALATE, OCTISALATE SEORIN COMPANY Co., Ltd. 4feb1010-469f-7e6e-e063-6394a90a9a9e 2026-05-14 Warnings Exact identifier application number: M020 Round Lab Summer Travel Kit AVOBENZONE, HOMOSALATE, OCTISALATE SEORIN COMPANY Co., Ltd. 4f8722e2-4636-e8ba-e063-6294a90a91e4 2026-05-14 Warnings Exact identifier application number: M020 La Roche Posay Anthelios UV Air Serum Sunscreen Broad Spectrum SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE L'Oreal USA Products Inc f3d841aa-b4fe-4a9d-8ad2-edd4445852d2 2026-05-14 Warnings Exact identifier application number: M020 Lancome Paris Renergie Lift MultiAction Sunscreen Broad Spectrum SPF 15 Firming AntiWrinkle AVOBENZONE, OCTISALATE AND OCTOCRYLENE L'Oreal USA Products Inc b746c24d-f775-4433-8519-49c3ec48ea0c 2026-05-14 Warnings Exact identifier application number: M020 LA ROCHE POSAY Laboratoire Dermatologique Cicaplast Balm B5 UV Skin Protectant Sunscreen Soothing Therapeutic Multi-Purpose Broad Spectrum SPF 50 DIMETHICONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE AND ZINC OXIDE LOreal USA Products Inc 92a1d6ce-aff3-45fc-8d98-20c4375aded8 2026-05-14 Warnings Exact identifier application number: M020 MELAO TALLOW SUNSCREEN ETHYLHEXYL METHOXYCINNAMATA,ETHYLHEXYL SALICYATE Guangzhou Haishi Biological Technology Co., Ltd. 519d9f52-b704-d6cd-e063-6294a90a6e42 2026-05-13 Warnings Exact identifier application number: M020 Hampton Sun SPF30 Mineral ZINX OXIDE S&C Hampton Sun LLC 019b0c1a-f9f3-4756-8b24-35bf4dc4aa22 2026-05-13 Warnings Exact identifier application number: M020 Standard Procedure SPF 50 Sunscreen Face and Body AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Baxter Laboratories 34f6150d-9627-94a5-e063-6394a90ad448 2026-05-13 Warnings Exact identifier application number: M020 CeraVe Developed with Dermotologists Ultra Light Moisturizing Broad Spectrum SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE L'Oreal USA Products Inc defa9588-95be-4f5c-86bb-53d6a1df7f5f 2026-05-13 Warnings Exact identifier application number: M020 MELAO TALLOW SUNSCREEN ETHYLHEXYL METHOXYCINNAMATE Guangzhou Haishi Biological Technology Co., Ltd. 22982b28-37df-ed81-e063-6394a90a77db 2026-05-12 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