AMMONIUM BENZOICUM- ammonium benzoate liquid 
Washington Homeopathic Products

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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DRUG FACTS

ACTIVE INGREDIENTS

AMMON BENZ

USES

To relieve the symptoms of the head feeling heavy.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

AMMON BENZ   Head feels heavy

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

DIRECTIONS

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

The OTC potency range of AMMON BENZ is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Label

All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

AMMONIUM BENZOICUM 
ammonium benzoate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-040
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMMONIUM BENZOATE (UNII: AC80WD7GPF) (AMMONIUM BENZOATE - UNII:AC80WD7GPF) AMMONIUM BENZOATE30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorwhite (white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71919-040-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product09/26/2012
2NDC:71919-040-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product09/26/2012
3NDC:71919-040-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/26/2012
4NDC:71919-040-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/26/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/26/2012
Labeler - Washington Homeopathic Products (084929389)
Establishment
NameAddressID/FEIBusiness Operations
Washington Homeopathic Products084929389manufacture(71919-040)

Revised: 12/2018
Document Id: 7e3ab47e-f1e6-f198-e053-2991aa0abdc8
Set id: d00627df-5858-43cd-b4cf-67c921cb9fe0
Version: 2
Effective Time: 20181230
 
Washington Homeopathic Products