ACETANILIDUM- acetanilide 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.

----------

DRUG FACTS

ACETANILIDE

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: 

ACETANILIDE   Fainting

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 ACETANILIDE 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 sazme 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.

ACETANILIDUM 
acetanilide liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-005
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETANILIDE (UNII: SP86R356CC) (ACETANILIDE - UNII:SP86R356CC) ACETANILIDE 30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color white (white) Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:71919-005-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/31/2012
2 NDC:71919-005-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 08/31/2012
3 NDC:71919-005-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/31/2012
4 NDC:71919-005-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 08/31/2012
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/31/2012
Labeler - Washington Homeopathic Products (084929389)
Establishment
Name Address ID/FEI Business Operations
Washington Homeopathic Products 084929389 manufacture(71919-005)

Revised: 12/2018
Document Id: 7e3e9fce-f2ee-8cc9-e053-2a91aa0aad73
Set id: a95b8311-7735-484b-8728-c2e16269bf36
Version: 2
Effective Time: 20181230
 
Washington Homeopathic Products