CERAVE DEVELOPED WITH DERMATOLOGISTS HEALING- petrolatum ointment 
L'Oreal USA Products Inc.

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Drug Facts

Active ingredient

Petrolatum 46.5%

Purpose

Skin protectant

Uses

• temporarily protects and helps relieve chafed, chapped or cracked skin

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

Inactive ingredients

mineral oil, paraffin, ozokerite, dimethicone, ceramide NP, ceramide AP, ceramide EOP, carbomer, water, sodium lauroyl lactylate, proline, cholesterol, phenoxyethanol, tocopheryl acetate, tocopherol, hydrolyzed hyaluronic acid, panthenol, pantolactone, phytosphingosine, xanthan gum, ethylhexylglycerin

Questions?

Toll-Free Number 1-888-768-2915

www.cerave.com

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CERAVE DEVELOPED WITH DERMATOLOGISTS HEALING 
petrolatum ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-500
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM46.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
PARAFFIN (UNII: I9O0E3H2ZE)  
CERESIN (UNII: Q1LS2UJO3A)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CERAMIDE 1 (UNII: 5THT33P7X7)  
CERAMIDE 3 (UNII: 4370DF050B)  
CERAMIDE 6 II (UNII: F1X8L2B00J)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
LAUROYL PROLINE (UNII: HDI505B669)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TOCOPHEROL (UNII: R0ZB2556P8)  
HYALURONIC ACID (UNII: S270N0TRQY)  
PANTHENOL (UNII: WV9CM0O67Z)  
PANTOLACTONE (UNII: J288D7O0JS)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-500-01340 g in 1 JAR; Type 0: Not a Combination Product09/20/2017
2NDC:49967-500-0285 g in 1 TUBE; Type 0: Not a Combination Product09/20/2017
3NDC:49967-500-03144 g in 1 TUBE; Type 0: Not a Combination Product09/20/2017
4NDC:49967-500-0415 in 1 TRAY09/20/2017
42.5 g in 1 JAR; Type 0: Not a Combination Product
5NDC:49967-500-0510 g in 1 TUBE; Type 0: Not a Combination Product09/20/2017
6NDC:49967-500-062 in 1 CARTON09/20/2017
610 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:49967-500-0753.6 g in 1 TUBE; Type 0: Not a Combination Product09/20/2017
8NDC:49967-500-081 in 1 BLISTER PACK09/20/2017
85 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01609/20/2017
Labeler - L'Oreal USA Products Inc. (002136794)
Establishment
NameAddressID/FEIBusiness Operations
Accupac, Inc.071609663MANUFACTURE(49967-500)

Revised: 12/2023
Document Id: 1c801d2d-efb6-497e-9c2d-9394436ec934
Set id: 1b3ad3e8-cbac-4a92-84e2-4f3ab4512d95
Version: 6
Effective Time: 20231231
 
L'Oreal USA Products Inc.