Oxalis 5: Homeopathic Product Information

OXALIS 5- oxalis stricta whole cream
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Directions: FOR TOPICAL USE ONLY.

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

Active Ingredient: Oxalis (Wood sorrel) 5X

Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Myrrh oil, Grapefruit seed extract

“prepared using rhythmical processes”

Use: Temporary relief of cramps.

KEEP OUT OF REACH OF CHILDREN.

Warnings: FOR EXTERNAL USE ONLY.
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. Natural ingredients may cause color and/or scent variation.

Questions? Call 866.642.2858
Made by with care by Uriel, East Troy, WI 53120
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Oxalis 5X Cream
(click image for full-size original)

OXALIS 5
oxalis 5 cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7148
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXALIS STRICTA WHOLE (OXALIS STRICTA WHOLE) OXALIS STRICTA WHOLE 5 [hp_X] in 1 g
Inactive Ingredients
Ingredient Name Strength
TEA TREE OIL
WATER
STEARIC ACID
ISOPROPYL MYRISTATE
LAVENDER OIL
CETYL ALCOHOL
POLYOXYL 40 STEARATE
STEARYL ALCOHOL
XANTHAN GUM
SORBIC ACID
FRANKINCENSE OIL
MYRRH OIL
CITRUS PARADISI SEED
Product Characteristics
Color white Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:48951-7148-5 60 g in 1 TUBE None
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 Operations
Uriel Pharmacy Inc. 043471163 manufacture (48951-7148)

Revised: 01/2024 Uriel Pharmacy Inc.

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