SOFTLIPS  WATERMELON- dimethicone stick 
The Mentholatum Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Dimethicone 2%

Purpose

Dimethicone - Skin protectant

Uses

Warnings

For external use only

When using this product

  • do not get into eyes

Stop use and ask a doctor if

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

Keep Out of Reach of Children

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

Directions

Inactive ingredients

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?

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

Package/Label Principal Display Panel

Softlips PDP

Package/Label Principal Display Panel

Drug Facts
SOFTLIPS   WATERMELON
dimethicone stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-7008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CERESIN (UNII: Q1LS2UJO3A)  
PETROLATUM (UNII: 4T6H12BN9U)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
SQUALANE (UNII: GW89575KF9)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
CASTOR OIL (UNII: D5340Y2I9G)  
MYRISTYL LACTATE (UNII: 1D822OC34X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MYRISTYL LAURATE (UNII: 58U0NZN2BT)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
LEVOMENTHOL (UNII: BZ1R15MTK7)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10742-7008-11 in 1 BLISTER PACK09/30/2019
12 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:10742-7008-22 in 1 BLISTER PACK10/15/2021
22 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/30/2019
Labeler - The Mentholatum Company (002105757)
Registrant - The Mentholatum Company (002105757)
Establishment
NameAddressID/FEIBusiness Operations
The Mentholatum Company002105757manufacture(10742-7008)

Revised: 2/2023
Document Id: f4204cef-2391-50bc-e053-2995a90ac851
Set id: e32d738e-e0af-4f17-a753-bdc7938b1684
Version: 3
Effective Time: 20230207
 
The Mentholatum Company