Home NDC 70707-400-01 Daily SPF30
Product NDC 70707-400
Requested package NDC 70707-400-01
11-digit product format 707070400
Labeler code 70707
Product ID 70707-400_d294b3fc-c64a-bd6d-e053-2995a90af6d3
Type HUMAN OTC DRUG
Nonproprietary name Octisalate 4.75%, Oxybenzone 4.25%, Octocrylene 2.80%, Avobenzone 3.005
Dosage form CREAM
Route TOPICAL
Labeler Face Reality Skin Care, LLC
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2012-05-03
Marketing end 0000-00-00
Substance OXYBENZONE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Active strength 0 g/g; g/g; g/g; g/g
NDC exclude flag No
Listing certified through 2022-12-31
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 · 4 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…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…
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70707-400 DAILY SPF30 (OCTISALATE 4.75%, OXYBENZONE 4.25%, OCTOCRYLENE 2.80%, AVOBENZONE 3.005) CREAM [FACE REALITY SKIN CARE, LLC] 8 Legacy NDC 20241205_3f2b463c-26a7-701f-e054-00144ff8d46c.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70707-400-01 70707040001 62.5 g in 1 TUBE (70707-400-01) 62.5 g 2012-05-03 0000-00-00 No No Current