Ars Alb: Homeopathic Product Information

ARS ALB- arsenic trioxide liquid
Energique, 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.

ACTIVE INGREDIENT:

(in each drop) Arsenicum Album 30C 100%.

PURPOSES:

Arsenicum Album — restlessness**

**Claims based on traditional homeopathic practices, not accepted medical evidence. Not FDA evaluated.

USES:

May temporarily relieve:

•restlessness •anxiety oversensitivity.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

Stop use and ask a doctor if symptoms persist for more than 7 days.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

• Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional.

• Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800-869-8078

PACKAGE LABEL DISPLAY:

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
ARS ALB

30C
1 fl. oz. (30 ml)

ARS ALB arsenicum album liquid

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0146 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARSENIC TRIOXIDE (ARSENIC CATION (3+)) ARSENIC CATION (3+) 30 [hp_C] in 1 mL

Inactive Ingredients Ingredient Name Strength WATER ALCOHOL

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:44911-0146-1 30 mL in 1 BOTTLE, DROPPER None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/12/2015

Labeler — Energique, Inc. (789886132)

Registrant — Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Operations
Apotheca Company		844330915	manufacture (44911-0146), api manufacture (44911-0146), label (44911-0146), pack (44911-0146)

Revised: 01/2023 Energique, Inc.