AMMONIUM BENZOICUM- ammonium benzoate pellet 
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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AMMONIUM BENZOICUM PELLETS

ACTIVE INGREDIENTS

AMMON BENZ 30C

USES

To relieve the symptoms of fainting.

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, stop use and consult your practitioner.

DIRECTIONS

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

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.

Ammon benz label example

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’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

AMMONIUM BENZOICUM 
ammonium benzoate pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68428-876
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMMONIUM BENZOATE (UNII: AC80WD7GPF) (AMMONIUM BENZOATE - UNII:AC80WD7GPF) AMMONIUM BENZOATE30 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Product Characteristics
Colorwhite (white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68428-876-0375 in 1 VIAL, GLASS; Type 0: Not a Combination Product09/26/2012
2NDC:68428-876-05150 in 1 VIAL, GLASS; Type 0: Not a Combination Product09/26/201212/04/2020
3NDC:68428-876-11300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/26/201212/04/2020
4NDC:68428-876-12600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/26/201212/04/2020
5NDC:68428-876-061200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/26/201212/04/2020
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(68428-876)

Revised: 12/2020
Document Id: b5afce94-1696-640f-e053-2a95a90ad327
Set id: 4f867e78-4910-4dfd-b427-a0756125e48d
Version: 2
Effective Time: 20201204
 
Washington Homeopathic Products