LOESCH ANTI-ITCH THERAPY- hydrocortisone liquid

Loesch by

Drug Labeling and Warnings

Loesch by is a Otc medication manufactured, distributed, or labeled by Loesch Laboratory Consultants, Inc., Bio-Medical & Pharmaceutical Manufacturing Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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. LabelNDC:

25280-004-02

LoeschAntiItchTherapy2oz.jpg

INGREDIENTS AND APPEARANCE

LOESCH  ANTI-ITCH THERAPY
hydrocortisone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 25280-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
LAURETH-4 (UNII: 6HQ855798J)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
BRUCINE SULFATE (UNII: KY7O12XPOQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 25280-004-02	59.147 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/26/2014

Labeler - Loesch Laboratory Consultants, Inc. (026619510)

Registrant - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)

Establishment
Name	Address	ID/FEI	Business Operations
Bio-Medical & Pharmaceutical Manufacturing Corporation		072186356	manufacture(25280-004)