SBS 41 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

Water, Cetyl Esters, Petrolatum, Isopropyl Palmitate, Phenoxyethanol, Stearyl Alcohol, Diazolidinyl Urea, Ceteareth-20, Carbomer, PEG-75 Lanolin, Hydroxyethylcellulose, Ethanolamine, Fragrance

SBS1L-DCN8808 SBS-40 Medicated Skin Cream-V6.jpg

SBS 40 Medicated Skin Cream

Silicone-free

Non-irritating

Non-greasy formulation

Helps heal dry hard-working hands

Industry's preferred brand for over 50 years

1 Liter

33.8 Fluid Ounces

40127

USDA Certified Biobased Product

Made in USA

Deb USA, Inc.

Charlotte, NC 28217-1388

1-800-248-7190

www.debgroup.com

Rev. 08-13

SBS1L-DCN8808 SBS-40 Medicated Skin Cream-V6.jpg

SBS 41 MEDICATED CREAM 
allantoin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-141
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CETYL ESTERS WAX (UNII: D072FFP9GU)  
PETROLATUM (UNII: 4T6H12BN9U)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
CARBOMER 934 (UNII: Z135WT9208)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
HYDROXYETHYL CELLULOSE (4000 CPS AT 1%) (UNII: ZYD53NBL45)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
MONOETHANOLAMINE (UNII: 5KV86114PT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-141-271000 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/201302/08/2023
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(11084-141)

Revised: 12/2020
Document Id: 4700289c-15f3-45a9-8a8a-da44ffff1df9
Set id: e842c501-5084-4955-a9e8-d34a5d73fcb0
Version: 3
Effective Time: 20201202
 
SC Johnson Professional USA, Inc.