Softlips Vanilla

Product NDC
10742-8508
11-digit product format
107428508
Labeler code
10742
Product ID
10742-8508_4dbef1d2-0153-3eaa-e063-6294a90a0cbc
Type
HUMAN OTC DRUG
Nonproprietary name
dimethicone
Dosage form
STICK
Route
TOPICAL
Labeler
The Mentholatum Company
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-10-03
Substance
DIMETHICONE
Active strength
20 mg/g
Pharmacologic classes
Skin Barrier Activity [PE]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Softlips Vanilla
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIMETHICONE20 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii92RU3N3Y1O

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-8508-1Softlips Vanilla2 g in 1 CYLINDERSTICK25
10742-8508-2Softlips Vanilla3 in 1 BLISTER PACKSTICK35
10742-8508-2Softlips Vanilla2 g in 1 TUBESTICK25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-8508SOFTLIPS VANILLA (DIMETHICONE) STICK [THE MENTHOLATUM COMPANY]4Current NDC, Legacy NDC, 3 package rows20241219_56551008-a4e0-406f-8403-980d2e6b75a0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-8508-1107428508012 g in 1 CYLINDER (10742-8508-1) 2 g2016-10-030000-00-00NoNoCurrent
10742-8508-2107428508023 TUBE in 1 BLISTER PACK (10742-8508-2) / 2 g in 1 TUBE3 tube2021-07-260000-00-00NoNoCurrent