NEOSPORIN ECZEMA ESSENTIALS  ANTI ITCH- hydrocortisone cream 
Johnson & Johnson Consumer Inc.

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.

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NEOSPORIN ® Eczema Essentials

Hydrocortisone Anti-Itch Cream

Drug Facts

Active ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Uses

  • temporarily relieves itching associated with minor skin irritations, inflammation, and rashes due to:
    • eczema
    • soaps
    • detergents
    • cosmetics
    • seborrheic dermatitis
    • psoriasis
  • other uses of this product should only be under the advice and supervision of a doctor

Warnings

For external use only.

Do not use for the treatment of diaper rash. Consult a doctor.

When using this product avoid contact with eyes

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, and do not begin use of any other hydrocortisone product unless you have asked a doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: do not use, ask a doctor

Other information

  • store at 20° to 25°C (68° to 77°F)

Inactive ingredients

water, petrolatum, glycerin, mineral oil, ceteareth-6, dimethicone, VP/eicosene copolymer, stearyl alcohol, phenoxyethanol, ammonium acryloyldimethyltaurate/VP copolymer, cetyl alcohol, carbomer, edetate disodium, methylparaben, sodium citrate, dipropylene glycol, ethylparaben, propylparaben, citric acid, ethylene brassylate, oat kernel extract, dihydrocitronellol, boswellia serrata resin extract, cis-3-hexenyl salicylate, sodium hydroxide 1

1
may contain this ingredient

Questions?

call 1-800-223-0182

DIST: JOHNSON & JOHNSON
CONSUMER PRODUCTS COMPANY
Division of Johnson & Johnson Consumer
Companies, Inc., Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

NEW
FROM THE #1 DOCTOR RECOMMENDED BRAND ®

NEOSPORIN ®
ECZEMA ESSENTIALS™

Hydrocortisone
Anti-itch Cream

Dual action formula

  • Fast relief of itch flare-
    ups due to eczema
  • Moisturizes to restore
    visibly healthier skin

Maximum Strength
Fragrance-free

RELIPID™
FORMULA
NET WT 1 OZ (28 g)

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
NEOSPORIN ECZEMA ESSENTIALS   ANTI ITCH
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-4010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
GLYCERIN (UNII: PDC6A3C0OX)  
MINERAL OIL (UNII: T5L8T28FGP)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
ETHYLPARABEN (UNII: 14255EXE39)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
OAT (UNII: Z6J799EAJK)  
3,7-DIMETHYLOCTANAL (UNII: F32WFZ5HGW)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58232-4010-28.5 g in 1 TUBE; Type 0: Not a Combination Product09/30/201112/01/2023
2NDC:58232-4010-11 in 1 CARTON09/30/201112/01/2023
228 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/30/201112/01/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: f37e2169-c54e-181a-e053-2a95a90a0a2c
Set id: dc9e9509-c2d4-4480-bbaa-009fc5ccf9fc
Version: 3
Effective Time: 20230130
 
Johnson & Johnson Consumer Inc.