NEOSPORIN ECZEMA ESSENTIALS ANTI ITCH- hydrocortisone cream

Neosporin Eczema Essentials by

Drug Labeling and Warnings

Neosporin Eczema Essentials by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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 hydroxide1

1 may contain this ingredient

Questions?

call 1-800-223-0182

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

NEOSPORIN ECZEMA ESSENTIALS   ANTI ITCH
hydrocortisone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58232-4010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hydrocortisone (UNII: WI4X0X7BPJ) (Hydrocortisone - UNII:WI4X0X7BPJ)	Hydrocortisone	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58232-4010-2	8.5 g in 1 TUBE; Type 0: Not a Combination Product	09/30/2011	12/01/2023
2	NDC: 58232-4010-1	1 in 1 CARTON	09/30/2011	12/01/2023
2		28 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 NOT FINAL	part348	09/30/2011	12/01/2023

Labeler - Johnson & Johnson Consumer Inc. (002347102)