Home NDC 70707-450-04 Daily SPF 30
Product NDC 70707-450
Requested package NDC 70707-450-04
11-digit product format 707070450
Labeler code 70707
Product ID 70707-450_d12b07c2-f782-0710-e053-2995a90ad29c
Type HUMAN OTC DRUG
Nonproprietary name OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Face Reality, Inc.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2016-06-20
Marketing end 0000-00-00
Substance OCTISALATE; OXYBENZONE; OCTOCRYLENE; AVOBENZONE
Active strength 48 mg/mL; mg/mL; mg/mL; mg/mL
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 70707-450 DAILY SPF 30 (OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE) CREAM [FACE REALITY, INC.] 4 Legacy NDC 20241205_7f05f7e4-153a-448a-be26-b66c4b9867b5.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70707-450-04 70707045004 118 mL in 1 BOTTLE (70707-450-04) 118 ml 2016-06-20 0000-00-00 No No Current