SOFTLIPS TROPICAL COCONUT PEACH PASSION- 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.

----------

Drug Facts

Active ingredients

Dimethicone 2%

Purpose

Dimethicone - Skin protectant

Uses

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

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

apply as needed

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 glycyrrhizate, BHT, menthol, tocopheryl acetatate [vitamin E]

Questions?

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

softlips.com

Package/Label Principal Display Panel

Package/Label Principal Display Panel

SOFTLIPS TROPICAL COCONUT PEACH PASSION
dimethicone stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10742-7005
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	20 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:10742-7005-1	2 in 1 BLISTER PACK	05/01/2020
1		2 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	05/01/2020

Labeler - The Mentholatum Company (002105757)

Registrant - The Mentholatum Company (002105757)

Name	Address	ID/FEI	Business Operations
Establishment
The Mentholatum Company		002105757	manufacture(10742-7005)