Oxalis 5X by Uriel Pharmacy, Inc OXALIS 5X ointment

Oxalis 5X by

Drug Labeling and Warnings

Oxalis 5X by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION

Apply to skin as needed. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredient: Oxalis (Wood sorrel) 5X

INACTIVE INGREDIENT

Inactive Ingredients: Sunflower seed oil, Lanolin, Water, Beeswax, Lanolin alcohol

Prepared using rhythmical processes.

PURPOSE

Use: Temporary relief of cramps.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

OXALIS 5X 
oxalis 5x ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-7224
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXALIS STRICTA WHOLE (UNII: 3STW243384) (OXALIS STRICTA WHOLE - UNII:3STW243384)	OXALIS STRICTA WHOLE	5 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN ALCOHOL (UNII: 884C3FA9HE)
WATER (UNII: 059QF0KO0R)
LANOLIN (UNII: 7EV65EAW6H)
BEESWAX (UNII: 2ZA36H0S2V)
SUNFLOWER OIL (UNII: 3W1JG795YI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-7224-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy, Inc (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy, Inc		043471163	manufacture(48951-7224)