Thuja occidentalis THUJA OCCIDENTALIS NEWTON LABORATORIES, INC. FDA Approved INDICATIONS & USAGE SECTION Warts; Brown spots on hand and arms; Vaccination effects; Dandruff; Diarrhea
FunFoxMeds box
Route
ORAL
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
OTC - ACTIVE INGREDIENT SECTION Thuja occidentalis 30c
Inactive Ingredients
INACTIVE INGREDIENT SECTION Inactive Ingredients: USP Purified Water; USP Gluten-free non-GMO organic cane alcohol 20%.
Treats Conditions
Indications Usage Section Warts Brown Spots On Hand And Arms Vaccination Effects Dandruff Diarrhea

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UPC
0788199555401
UNII
1NT28V9397
Packaging

PACKAGE LABEL package label

Package Descriptions
  • PACKAGE LABEL package label

Overview

INDICATIONS & USAGE SECTION Warts; Brown spots on hand and arms; Vaccination effects; Dandruff; Diarrhea

Indications & Usage

INDICATIONS & USAGE SECTION Warts; Brown spots on hand and arms; Vaccination effects; Dandruff; Diarrhea

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) as needed or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Warnings & Precautions
WARNINGS SECTION Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
Purpose

OTC - PURPOSE SECTION Warts; Brown spots on hand and arms; Vaccination effects; Dandruff; Diarrhea

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION Keep out of reach of children.

Questions

QUESTIONS SECTION newtonlabs.net – Questions? 800.448.7256 Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013


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