SBS 40 MEDICATED CREAM- allantoin cream 
SC Johnson Professional USA, Inc.

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 ingredient

Allantoin, 0.5%

Purpose

Skin protectant

Uses

temporarily protects and helps relieve chapped or cracked skin

helps protect from the drying effects of wind and cold weather

Warnings

For external use only

Do not use on

deep or puncture wounds

animal bites

serious burns

When using this product

avoid contact with eyes.

In case of eye contact, flush with water.

Stop use and ask a doctor if

irritation or sensitivity develops

condition worsens

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

Keep out of reach of children

Directions

apply to clean, dry hands as needed

rub in well

Inactive ingredients

AQUA (WATER), CETYL ESTERS, PETROLATUM, ISOPROPYL PALMITATE, STEARYL ALCOHOL, CARBOMER, CETEARETH-20, CHLOROXYLENOL, METHYLPARABEN, LANOLIN, SODIUM HYDROXIDE, PROPYLPARABEN, PARFUM (FRAGRANCE).

SBS100ML-SBS-40 Medicated Skin Cream-V5b.jpg

SBS100ML-SBS-40 Medicated Skin Cream-V5b.jpg

deb stoko

SBS-40

Medicated Skin Cream

Normal Skin

Crema medicada para la piel

Piel normal

EN Skin conditioning cream. Ideal for irritated skin.

Non-greasy. Non-irritating.

ES Acondicionador para la piel. Ideal para la piel

irritada. No es grasiento. No es irritante.

100 ml (3.38 fl oz)

Stock #:

SBS100ML

DCN8807/0115

Deb USA, Inc.

Charlotte, NC 28217

1-800-248-7190

www.debgroup.com Made in USA

SBS 40 MEDICATED CREAM 
allantoin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-241
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
CARBOMER 934 (UNII: Z135WT9208)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
CHLOROXYLENOL (UNII: 0F32U78V2Q)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
LANOLIN (UNII: 7EV65EAW6H)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-241-082500 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/201306/30/2021
2NDC:11084-241-35148 mL in 1 TUBE; Type 0: Not a Combination Product12/01/201304/01/2018
3NDC:11084-241-3930 mL in 1 TUBE; Type 0: Not a Combination Product12/01/201301/28/2023
4NDC:11084-241-10100 mL in 1 TUBE; Type 0: Not a Combination Product06/01/201502/03/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34711/01/201312/31/2023
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
SC Johnson Professional USA, Inc.078805627manufacture(11084-241)

Revised: 12/2020
 
SC Johnson Professional USA, Inc.