OXALTEM- berberis vulgaris, oxalicum acidum, sanguinaria canadensis, chimaphila umbellata, calcarea fluorica, calcarea silicata, uricum acidum, calcarea phosphorica, parathormonum, pyridoxinum hydrochloricum liquid

Oxaltem by

Drug Labeling and Warnings

Oxaltem by is a Homeopathic medication manufactured, distributed, or labeled by Nucleic Products, LLC, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Berberis Vulgaris 6X, 9X, 12X, Calcarea Fluorica 12X 30C, Calcarea Phosphorica 6C, 9C, 30C, Calcarea Silicata 12X 30C, Chimaphila Umbellata 9X, 30C, Oxalicum Acidum 6X, 9X, 12X, 30C, Parathormonum 9C, Pyridoxinum Hydrochloricum 12C, Sanguinaria Canadensis 9X, Uricum Acidum 12X, 30C.

PURPOSE:

Berberis Vulgaris – Temporary relief of joint pain, Calcarea Fluorica - Temporary relief of bone pain, Calcarea Phosphorica - Temporary relief of back weakness, Calcarea Silicata - Temporary relief of skin itching, Chimaphila Umbellata - Temporary relief of urinary pain, Oxalicum Acidum - Temporary relief of back pain, Parathormonum – Parathyroid support, Pyridoxinum Hydrochloricum – Energy regulation, Sanguinaria Canadensis - Temporary relief of headaches, Uricum Acidum - Temporary relief of skin itching

USES:

Homeopathic remedy that regulates oxalate in the body.

*These "uses" have not been evaluated by the Food and Drug Administration.

**C, K, CK, and X are homeopathic dilutions see www.hpus.com

WARNINGS:

As with any drug, ask a doctor before use if pregnant or nursing.

Consult a physician if: Symptoms persist for more than 7 days or worsen.

Keep this and all medications out of the reach of children.

In case of accidental overdose, contact a medical professional or poison control center immediately.

Do not use if seal is broken or missing.

This Product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten, soy, or milk derivatives.

KEEP OUT OF REACH OF CHILDREN:

In case of accidental overdose, contact a medical professional or poison control center immediately.

DIRECTIONS:

Adults and children 12 years of age and older: Take 1 full eyedropper twice a day to help alleviate symptoms of neurological disorders.

Under 12 years of age: Consult a physician.

INACTIVE INGREDIENTS

20% organic ethanol, purified water

QUESTIONS:

Distributed By:

Nucleic Products, LLC

PO Box 7148 Grove, OK 74344

Call weekdays 9am-5pm (918)791-1727

PACKAGE LABEL DISPLAY:

NDC: 75053-0012-1

Nu cleic

Oxaltem

Homeopathic Medicine

For Professional Use Only

4 fl oz. (118 ml)

INGREDIENTS AND APPEARANCE

OXALTEM 
berberis vulgaris, oxalicum acidum, sanguinaria canadensis, chimaphila umbellata, calcarea fluorica, calcarea silicata, uricum acidum, calcarea phosphorica, parathormonum, pyridoxinum hydrochloricum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75053-0012
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U)	BERBERIS VULGARIS ROOT BARK	6 [hp_X]  in 1 mL
OXALIC ACID DIHYDRATE (UNII: 0K2L2IJ59O) (OXALIC ACID - UNII:9E7R5L6H31)	OXALIC ACID DIHYDRATE	6 [hp_X]  in 1 mL
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	9 [hp_X]  in 1 mL
CHIMAPHILA UMBELLATA WHOLE (UNII: WCK21A9W9J) (CHIMAPHILA UMBELLATA - UNII:WCK21A9W9J)	CHIMAPHILA UMBELLATA WHOLE	9 [hp_X]  in 1 mL
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)	CALCIUM FLUORIDE	12 [hp_X]  in 1 mL
CALCIUM SILICATE (UNII: S4255P4G5M) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SILICATE	12 [hp_X]  in 1 mL
URIC ACID (UNII: 268B43MJ25) (URIC ACID - UNII:268B43MJ25)	URIC ACID	12 [hp_X]  in 1 mL
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	6 [hp_C]  in 1 mL
PARATHYROID HORMONE (UNII: N19A0T0E5J) (PARATHYROID HORMONE - UNII:N19A0T0E5J)	PARATHYROID HORMONE	9 [hp_C]  in 1 mL
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z)	PYRIDOXINE	12 [hp_C]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75053-0012-1	118 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/21/2024

Labeler - Nucleic Products, LLC (117470417)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(75053-0012) , api manufacture(75053-0012) , label(75053-0012) , pack(75053-0012)