Label: 3-IN-1 RELIEF CVS- colloidal oatmeal - 1.00% lotion
-
Contains inactivated NDC Code(s)
NDC Code(s): 59779-451-05 - Packager: CVS
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated December 8, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient Purpose
- Uses
- Warning
- DOSAGE & ADMINISTRATION
-
Inactive ingredients
Water, Glycerin, Distearyldimonium Chloride, Petrolatum, Panthenol, Isopropyl Palmitate, Cetyl Alcohol, Dimethicone, Avena Sativa (Oat) , Kernel Oil, Avena Sativa (Oat) Kernel Extract, Cucumis Sativus (Cucumber) Fruit Extract, Aloe Barbadensis Leaf Extract, Chamomilla Recutita , Matricaria) Flower Extract, Ceramide NP, Sorbitol, Lecithin, Xanthan Gum, Oleic Acid, Iron Oxides, Sodium Chloride, Steareth-20, Pentylene , Glycol, 4-t-Butylcyclohexanol, Propylene Glycol, Benzalkonium Chloride
- PURPOSE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
3-IN-1 RELIEF CVS
colloidal oatmeal - 1.00% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-451 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 1.0 g in 100 g Inactive Ingredients Ingredient Name Strength 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) Dimethicone (UNII: 92RU3N3Y1O) Cucumber (UNII: YY7C30VXJT) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) CERAMIDE NP (UNII: 4370DF050B) Sorbitol (UNII: 506T60A25R) Xanthan Gum (UNII: TTV12P4NEE) Oleic Acid (UNII: 2UMI9U37CP) FERROUS OXIDE (UNII: G7036X8B5H) Sodium Chloride (UNII: 451W47IQ8X) Steareth-20 (UNII: L0Q8IK9E08) Pentylene Glycol (UNII: 50C1307PZG) 4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C) Propylene Glycol (UNII: 6DC9Q167V3) Benzalkonium Chloride (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-451-05 170 g in 1 BOTTLE; Type 0: Not a Combination Product 11/30/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/30/2015 Labeler - CVS (062312574) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(59779-451) , label(59779-451)