THUJA OCCIDENTALIS - thuja occidentalis pellet 
Newton Laboratories, 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.

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Thuja occidentalis

INDICATIONS & USAGE SECTION

Warts; Brown spots on hand & arms; Ovarian cysts; Vaccination effects; Dandruff; Diarrhea.

DOSAGE & ADMINISTRATION SECTION

Directions:  Ages 12 and up, take 6 pellets by mouth (ages 0 to 11, give 3 pellets) as needed or as directed by a health professional.  Under age 2, crush/dissolve pellets in purified water.  Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

 Thuja occidentalis 15x, 10x, 200c, 30c.

OTC - PURPOSE SECTION

Warts; Brown spots on hand & arms; Ovarian cysts; Vaccination effects; Dandruff; Diarrhea.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Gluten-free, non-GMO, organic beet-derived sucrose (lactose free) pellets.

QUESTIONS SECTION

www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions? 1.800.448.7256

WARNINGS SECTION

WARNINGS:  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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

package image

THUJA OCCIDENTALIS  
thuja occidentalis pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55714-7540
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Thuja Occidentalis Leafy Twig (UNII: 1NT28V9397) (Thuja Occidentalis Leafy Twig - UNII:1NT28V9397) Thuja Occidentalis Leafy Twig15 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
Sucrose (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55714-7540-128 g in 1 BOTTLE, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2011
Labeler - Newton Laboratories, Inc. (788793610)
Registrant - Newton Laboratories, Inc. (788793610)
Establishment
NameAddressID/FEIBusiness Operations
Newton Laboratories, Inc.788793610MANUFACTURE(55714-7540)

Revised: 9/2011
Document Id: dbdbfe9b-b84a-cf6b-3774-4f1f46c934ea
Set id: b197e2dd-4b5e-2da9-7f5d-27e6c6ec782c
Version: 1
Effective Time: 20110901
 
Newton Laboratories, Inc.