FDA.reportPublic FDA data

Softlips Oasis Strawberry Kiwi

Product NDC
10742-8746
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct10742-8746DDiscontinued by firm2026-09-14
excluded packagepackage10742-874610742-8746-1DDiscontinued by firm2026-09-14
excluded packagepackage10742-874610742-8746-2DDiscontinued by firm2026-09-14

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 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage10742-8746-2d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage10742-8746-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage10742-8746-2f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage10742-8746-1f5e01cc5f278…a2eaf40c39c3…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
10742-8746-12023-02-07Drug Facts - Softlips Oasis Strawberry Kiwi
10742-8746-22023-02-07Drug Facts - Softlips Oasis Strawberry Kiwi
10742-8746-12023-01-30Drug Facts - Softlips Oasis Strawberry Kiwi
10742-8746-22023-01-30Drug Facts - Softlips Oasis Strawberry Kiwi

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-8746-1107428746011 TUBE in 1 BLISTER PACK (10742-8746-1) > 4.5 g in 1 TUBE1 tube2019-05-010000-00-00NoNoCurrent
10742-8746-2107428746024.5 g in 1 TUBE (10742-8746-2) 4.5 g2019-07-150000-00-00NoNoCurrent