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Amnion Oxalis Comp.

Amnion Oxalis Comp. is an over-the-counter drug, made by Uriel Pharmacy, Inc.

Type
Over the counter
Drug class
Not classified
Route
Oral
Manufacturers
1

Directions: FOR ORAL USE ONLY.

Drug facts

Name
Amnion Oxalis Comp.
Active ingredients
Amniotic Fluid (Bovine), Kalanchoe Daigremontiana Leaf, Oxalis Stricta Whole
Dosage forms
Liquid
Label holder
Uriel Pharmacy, Inc
Label updated
02/06/2025

Active ingredients

Bryophyllum e fol. (Life plant) 3X, Oxalis e pl. tota (Wood sorrel) 3X, Amnion (Bovine fetus amniotic membrane) 30X

Purpose

Use: Temporary relief of headache.

Uses

Directions: FOR ORAL USE ONLY.

Directions

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

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 or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN.

Inactive ingredients

Distilled water, 30% Organic cane alcohol Prepared using rhythmical processes.

Questions?

Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 shopuriel.com Lot:

Forms and strengths

From the FDA NDC Directory · 1 product codes

Dosage formStrengthRouteNDCs
Liquid3 [hp_X]/mL / 30 [hp_X]/mL / 3 [hp_X]/mLoral1

Manufacturers and labels

1 FDA label

  • Uriel Pharmacy, IncShown hereLabel 02/06/2025 · NDC 48951-1396Full label

Related recalls

No FDA enforcement reports name Amnion Oxalis Comp. or its active ingredient.

Amnion Oxalis Comp.: common questions

What is Amnion Oxalis Comp. used for?
Directions: FOR ORAL USE ONLY.
Is Amnion Oxalis Comp. a prescription drug?
No. Amnion Oxalis Comp. is sold over the counter (OTC) without a prescription.
Who makes Amnion Oxalis Comp.?
Uriel Pharmacy, Inc lists Amnion Oxalis Comp. with the FDA.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 02/06/2025 · Label text is shown as published by the manufacturer. Not medical advice