Softlips

Manufacturer
The Mentholatum Company
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:44:20

Label at a glance#

ProductSoftlips Watermelon
Active ingredientDIMETHICONE
Label structure10 sections

Indications and uses

temporarily protects and helps relieve chapped or cracked lips helps protect from the drying effects of wind and cold weather

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 2%

Purpose

OTC - PURPOSE SECTION

Dimethicone - Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • temporarily protects and helps relieve chapped or cracked lips
  • helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

ozokerite, petrolatum, ethylhexyl palmitate, squalane, octyldodecanol, myristyl myristate, ricinus communis (castor) seed oil, myristyl lactate, cetyl alcohol, flavor, myristyl laurate, myristyl alcohol, ammonium glycrrhizate, BHT, menthol, tocopheryl acetatate [vitamin E]

Questions?

OTC - QUESTIONS SECTION

1-877-636-2677 MON-FRI 9AM to 5PM (EST)

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Softlips PDP
Softlips PDP

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts
Drug Facts

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10742-7008-12023-02-07C16284748780-1f386c649-df15-0266-e053-dadaa90a7c1aDrug Facts
10742-7008-22023-02-07C16284748780-1f386c649-df15-0266-e053-dadaa90a7c1aDrug Facts
10742-7008-12023-01-30C16284748780-1f386c649-df15-0266-e053-dadaa90a7c1aDrug Facts
10742-7008-22023-01-30C16284748780-1f386c649-df15-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-7008-1SoftlipsWatermelon1 in 1 BLISTER PACKSTICK14
10742-7008-1SoftlipsWatermelon2 g in 1 TUBESTICK24
10742-7008-2SoftlipsWatermelon2 in 1 BLISTER PACKSTICK24
10742-7008-2SoftlipsWatermelon2 g in 1 TUBESTICK24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-7008SOFTLIPS WATERMELON (DIMETHICONE) STICK [THE MENTHOLATUM COMPANY]4Current NDC, Legacy NDC, 4 package rows20241219_e32d738e-e0af-4f17-a753-bdc7938b1684.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-700810742-7008-1, 10742-7008-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Softlips WatermelonDIMETHICONEThe Mentholatum Companye32d738e-e0af-4f17-a753-bdc7938b16842024-12-17WarningsExact identifier
ndc (package): 10742-7008-1
ndc (package): 10742-7008-2
ndc (product): 10742-7008
ndc11 (package): 10742700801
ndc11 (package): 10742700802
spl id: 2978c10c-077d-152a-e063-6394a90af864
spl set id: e32d738e-e0af-4f17-a753-bdc7938b1684

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.