Sween 24

Dosage form: cream
Ingredients: DIMETHICONE 60mg in 1g
Labeler: Coloplast Manufacturing US, LLC
NDC code: 11701-063

Medically reviewed by Drugs.com. Last updated on Feb 12, 2024.

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

apply as needed

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)

SWEEN 24
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11701-063
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (DIMETHICONE)	DIMETHICONE	60 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
BEHENTRIMONIUM METHOSULFATE
CETOSTEARYL ALCOHOL
ETHYLHEXYL PALMITATE
GLYCERIN
ISOPROPYL PALMITATE
PEG-150 PENTAERYTHRITYL TETRASTEARATE
WATER

Packaging
#	Item Code	Package Description
1	NDC:11701-063-71	142 g in 1 TUBE
2	NDC:11701-063-70	256 g in 1 TUBE
3	NDC:11701-063-73	57 g in 1 TUBE
4	NDC:11701-063-72	4 g in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part347	06/15/2009

Labeler - Coloplast Manufacturing US, LLC (110326675)

Registrant - Coloplast Corp (847436391)

Establishment
Name	Address	ID/FEI	Operations
Coloplast Manufacturing US, LLC		110326675	MANUFACTURE(11701-063)

Document Id: 740e64dc-82ce-4d48-a6b9-4be17a01518f

Set id: a623c8d7-8db0-410a-9980-02ac02f7b6ea

Version: 6

Effective Time: 20180221

Coloplast Manufacturing US, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer