DIABETIC RELIEF CVS- dimethicone lotion 
CVS

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 ingredient                            Purpose

Dimethicone 1%.................................Skin Protectant

Uses

 temporarily protects and helps chapped or cracked skin

Warning

For external use only.
Do not use on • deep puncture wounds• animal bites • serious burns

When using this product • do not get into eyes. Rinse with water to remove

Stop use and ask a doctor if • condition worsens • symptoms persist for 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 immediately.

Directions • Apply as needed

Inactive ingredients

Water, Glycerin, Distearyldimonium Chloride, Petrolatum, Panthenol, Isopropyl Palmitate, Cetyl Alcohol, Avena Sativa (Oat) Kernel Oil, Avena , Sativa (Oat) Kernel Extract, Sorbitol, Lecithin, Xanthan Gum, Oleic Acid, Iron Oxide, Phenoxyethanol, Ethylhexylglycerin, Steareth-20, Sodium Chloride, Colloidal Oatmeal, Propylene Glycol, Cucumis Sativus (Cucumber) Fruit Extract, Pentylene Glycol, 4-t-Butylcyclohexanol, Benzalkonium Chloride, Chamomilla Recutita (Matricaria) Flower Extract, Aloe Barbadensis Leaf Extract, Ceramide NP

image descriptionimage description

DIABETIC RELIEF  CVS
dimethicone - 1.0% lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-437
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Distearyldimonium Chloride (UNII: OM9573ZX3X)  
Petrolatum (UNII: 4T6H12BN9U)  
Panthenol (UNII: WV9CM0O67Z)  
Isopropyl Palmitate (UNII: 8CRQ2TH63M)  
Cetyl Alcohol (UNII: 936JST6JCN)  
OAT KERNEL OIL (UNII: 3UVP41R77R)  
OAT (UNII: Z6J799EAJK)  
Sorbitol (UNII: 506T60A25R)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
Xanthan Gum (UNII: TTV12P4NEE)  
Oleic Acid (UNII: 2UMI9U37CP)  
BROWN IRON OXIDE (UNII: 1N032N7MFO)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Steareth-20 (UNII: L0Q8IK9E08)  
Sodium Chloride (UNII: 451W47IQ8X)  
OATMEAL (UNII: 8PI54V663Y)  
Propylene Glycol (UNII: 6DC9Q167V3)  
CUCUMBER (UNII: YY7C30VXJT)  
Pentylene Glycol (UNII: 50C1307PZG)  
4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)  
Benzalkonium Chloride (UNII: F5UM2KM3W7)  
CHAMOMILE (UNII: FGL3685T2X)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CERAMIDE NP (UNII: 4370DF050B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-437-05170 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34711/30/201512/01/2015
Labeler - CVS (062312574)
Registrant - Product Quest Mfg (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg927768135manufacture(59779-437) , label(59779-437)

Revised: 9/2015
 
CVS