Home NDC 10742-8746-2 Softlips Oasis Strawberry Kiwi
Product NDC 10742-8746
Requested package NDC 10742-8746-2
11-digit product format 107428746
Labeler code 10742
Product ID 10742-8746_08ef87ac-fa34-487b-9cf9-b7c4ba4b95d0
Type HUMAN OTC DRUG
Nonproprietary name dimethicone, oxybenzone, octinoxate
Dosage form STICK
Route TOPICAL
Labeler The Mentholatum Company
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2019-05-01
Marketing end 0000-00-00
Substance DIMETHICONE; OCTINOXATE; OXYBENZONE
Active strength 20 mg/g; mg/g; mg/g
NDC exclude flag No
Listing certified through 2020-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 10742-8746 10742-8746-2 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 10742-8746 10742-8746-2 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10742-8746-2 10742874602 4.5 g in 1 TUBE (10742-8746-2) 4.5 g 2019-07-15 0000-00-00 No No Current