Home NDC 70367-007-01 Oil Free Matte Sunscreen SPF 30, - Zinc Oxide, Octinoxate, Octisalate, Oxybenzone
Product NDC 70367-007
Requested package NDC 70367-007-01
11-digit product format 703670007
Labeler code 70367
Product ID 70367-007_9cd5746c-8c92-918b-e053-2995a90ada7a
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Octinoxate, Octisalate, Oxybenzone
Dosage form LOTION
Route TOPICAL
Labeler Only Yourx, Inc.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2014-08-26
Marketing end 0000-00-00
Substance OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE
Active strength 7 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70367-007-01 Oil Free Matte Sunscreen SPF 30, - Zinc Oxide, Octinoxate, Octisalate, Oxybenzone 30 mL in 1 TUBE LOTION 30 4 70367-007-04 Oil Free Matte Sunscreen SPF 30, - Zinc Oxide, Octinoxate, Octisalate, Oxybenzone 120 mL in 1 TUBE LOTION 120 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70367-007 OIL FREE MATTE SUNSCREEN SPF 30, - ZINC OXIDE, OCTINOXATE, OCTISALATE, OXYBENZONE (ZINC OXIDE, OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [ONLY YOURX, INC.] 4 Legacy NDC, 2 package rows 20200124_76444f6a-1d87-44cc-e053-2a91aa0a43d6.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70367-007-01 70367000701 30 mL in 1 TUBE (70367-007-01) 30 ml 2014-08-26 0000-00-00 No No Current