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Loesch Anti-Itch Therapy

Dosage form: liquid
Ingredients: HYDROCORTISONE 5mg in 1mL
Labeler: Loesch Laboratory Consultants, Inc.
NDC Code: 25280-004

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.

Loesch Anti-Itch Therapy

Active Ingredient

Hydrocortisone, USP (0.5%)

Purpose

Anti-Itch

Use
  • Specially formulated to rapidly and completely penetrate the scalp (or skin) delivering itch relief anywhere it's needed.
  • This liquid preparation can be applied to the skin or scalp to temporarily relieve minor itching and skin irritations commonly associated with insect bites, poison oak, poison sumac, and skin blemishes.

Warnings
  • Not for use on children under 2 years old except as directed by a pediatrician.
  • Avoid contact with eyes and mucous membranes.
  • Do not apply to large areas of the body and do not use for extended periods of time.
  • For external use only.
  • If irritation develops and persists, discontinue use and ask a doctor.
  • When using this product, if condition worsens or if symptoms persists for more than 7 days or clear up and occur again within a few days, stop use and ask a doctor.

Keep out of reach of children.

Directions
  • Apply this product topically to affected areas and allow to dry without rubbing.
  • Use up to 3 times daily.
  • Use only as directed.

Other Information
  • External antipruritic

Inactive Ingredients:

Ethanol, Purified Water, Isopropyl Alcohol, Glycerin, Laureth 4, t-Butyl Alcohol, Brucine Sulfate

Questions or Comments?

Loesch Laboratory Consultants, Inc.
4311 South Dr., Houston, TX 77053-4820
800.231.7157 M-F 8am-5pm

Image of 2.0 Fl. Oz. Label
NDC:25280-004-02

LoeschAntiItchTherapy2oz.jpg

LOESCH  ANTI-ITCH THERAPY
hydrocortisone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25280-004
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (HYDROCORTISONE) HYDROCORTISONE5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
WATER 
ISOPROPYL ALCOHOL 
GLYCERIN 
LAURETH-4 
TERT-BUTYL ALCOHOL 
BRUCINE SULFATE 
Packaging
#Item CodePackage Description
1NDC:25280-004-0259.147 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/26/2014
Labeler - Loesch Laboratory Consultants, Inc. (026619510)
Registrant - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)
Establishment
NameAddressID/FEIOperations
Bio-Medical & Pharmaceutical Manufacturing Corporation072186356manufacture(25280-004)

Revised: 06/2014
 
Loesch Laboratory Consultants, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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