CERAVE DEVELOPED WITH DERMATOLOGISTS BABY MOISTURIZING- dimethicone lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Dimethicone 1%

Purpose

Skin protectant

Uses

temporarily protects and helps relieve chafed, chapped, or cracked skin
helps protect from the drying effects of wind and cold weather

Warnings

For external use only

Do not use on

When using this product

do not get into eyes

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

apply as needed

Other information

Inactive ingredients

purified water, caprylic/capric triglyceride, cetostearyl alcohol, cetyl alcohol, emulsifying wax, phenoxyethanol,niacinamide, ceramide 3, ceramide 6-II, ceramide 1, hyaluronic acid, allantoin, tocopheryl acetate, lauric acid, zinc citrate, polyglyceryl-3 diisostearate, bBehentrimonium methosulfate, sodium lauroyl lactylate, arginine PCA, potassium phosphate, dipotassium phosphate, EDTA, sodium PCA, phytosphingosine, cholesterol, xanthan gum, carbomer, ethylhexylglycerin

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CERAVE DEVELOPED WITH DERMATOLOGISTS BABY MOISTURIZING 
dimethicone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-190
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
NIACINAMIDE (UNII: 25X51I8RD4)  
CERAMIDE 3 (UNII: 4370DF050B)  
CERAMIDE 6 II (UNII: F1X8L2B00J)  
HYALURONIC ACID (UNII: S270N0TRQY)  
ALLANTOIN (UNII: 344S277G0Z)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LAURIC ACID (UNII: 1160N9NU9U)  
ZINC CITRATE (UNII: K72I3DEX9B)  
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)  
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)  
EDETIC ACID (UNII: 9G34HU7RV0)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-190-01237 mL in 1 BOTTLE; Type 0: Not a Combination Product08/17/201705/31/2024
2NDC:49967-190-0229 mL in 1 BOTTLE; Type 0: Not a Combination Product08/17/201705/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01608/17/201705/31/2024
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA Products, Inc.624244349MANUFACTURE(49967-190)

Revised: 1/2024
Document Id: e1b5b225-a52b-42de-b4f1-afe131bb7b22
Set id: 81c58dbd-6c36-424f-b487-a85f54c28f44
Version: 5
Effective Time: 20240129
 
L'Oreal USA Products Inc