CERAVE DEVELOPED WITH DERMATOLOGISTS HEALING- petrolatum ointment

Cerave Developed with Dermatologists Healing by

Drug Labeling and Warnings

Cerave Developed with Dermatologists Healing by is a Otc medication manufactured, distributed, or labeled by L’Oreal USA Products Inc, Accupac, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Petrolatum 49.5%

Purpose

Skin protectant

Uses

temporarily protects minor:

    cuts scrapes burns

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

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

do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last 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 right away.

Directions

apply as needed

Inactive ingredients

mineral oil, microcrystalline wax, glycerin, paraffin, synthetic wax,
ceramide NP, ceramide AP, ceramide EOP, carbomer, water, triethyl
citrate, sodium lauroyl lactylate, sodium hyaluronate, cholesterol,
tocopheryl acetate, tocopherol, caprylyl glycol, panthenol,
phytosphingosine, xanthan gum, benzoic acid

Questions or comments?

Toll-free number 1-888-768-2915

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INGREDIENTS AND APPEARANCE

CERAVE DEVELOPED WITH DERMATOLOGISTS HEALING 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-721
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	495 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
GLYCERIN (UNII: PDC6A3C0OX)
PARAFFIN (UNII: I9O0E3H2ZE)
CERAMIDE NP (UNII: 4370DF050B)
CERAMIDE AP (UNII: F1X8L2B00J)
CARBOMER (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CHOLESTEROL (UNII: 97C5T2UQ7J)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PANTHENOL (UNII: WV9CM0O67Z)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
XANTHAN GUM (UNII: TTV12P4NEE)
BENZOIC ACID (UNII: 8SKN0B0MIM)
SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-721-01	85 g in 1 TUBE; Type 0: Not a Combination Product	11/01/2025
2	NDC: 49967-721-02	144 g in 1 TUBE; Type 0: Not a Combination Product	11/01/2025
3	NDC: 49967-721-03	340 g in 1 JAR; Type 0: Not a Combination Product	11/01/2025
4	NDC: 49967-721-04	54 g in 1 TUBE; Type 0: Not a Combination Product	11/01/2025
5	NDC: 49967-721-05	15 in 1 CARTON	11/01/2025
5		2.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/01/2025

Labeler - L’Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
Accupac, LLC		061595175	manufacture(49967-721) , pack(49967-721)