SWEEN 24- dimethicone cream 
Coloplast Manufacturing US, LLC

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Sween® 24

Drug Facts

Active ingredient

Dimethicone, 6%

Purpose

Skin Protectant

Uses

Helps prevent and temporarily protects chafed, chapped or cracked skin and lips.

Warnings

For external use only.

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • Do not get into eyes

Stop using this product if

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

Keep this and all drugs out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

Inactive ingredients

behentrimonium methosulfate, cetearyl alcohol, ethylhexyl palmitate, glycerin, isopropyl palmitate, PEG-5 ditrimethylolpropane tetrahydroxystearate, PEG-150 pentaerythrityl tetrastearate, water

Questions or comments?

Call toll free 1-800-533-0464

Manufactured by: Coloplast A/S, Holtedam 1,
DK-3050 Humlebaek, Denmark
Distributed by: Coloplast Corp, 1601 W River Rd N,
Minneapolis, MN 55411 U.S.A.

PRINCIPAL DISPLAY PANEL - 57 g Tube Label

NDC 11701-063-73

Sween® 24

Moisturizer
Once a Day
Moisturizing
Body Cream

For Normal to Dry,
Flaky, Itchy Skin

Product #7091

Coloplast

NET WT. 2 OZ. (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Tube Label
SWEEN 24 
dimethicone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11701-063
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE60 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11701-063-71142 g in 1 TUBE; Type 0: Not a Combination Product06/15/2009
2NDC:11701-063-70256 g in 1 TUBE; Type 0: Not a Combination Product06/15/2009
3NDC:11701-063-7357 g in 1 TUBE; Type 0: Not a Combination Product06/15/2009
4NDC:11701-063-724 g in 1 PACKET; Type 0: Not a Combination Product06/15/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01606/15/2009
Labeler - Coloplast Manufacturing US, LLC (110326675)
Registrant - Coloplast Corp (847436391)
Establishment
NameAddressID/FEIBusiness Operations
Coloplast Manufacturing US, LLC110326675MANUFACTURE(11701-063)

Revised: 12/2023
Document Id: 49cacdf2-8886-4e1f-9e7b-69e4a415a70f
Set id: a623c8d7-8db0-410a-9980-02ac02f7b6ea
Version: 8
Effective Time: 20231221
 
Coloplast Manufacturing US, LLC