ARSENICUM SULPHURATUM FLAVUM- arsenic trisulfide 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

ARSENICUM SULPHURATUM FLAVUM

USES

To relieve the symptoms of itchy skin.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

ARSENICUM SULPHURATUM FLAVUM   Itchy skin

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 ARSENICUM SULPHURATUM FLAVUM is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM.
Label
Availability is subject to change.

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.

ARSENICUM SULPHURATUM FLAVUM 
arsenic trisulfide liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-087
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARSENIC TRISULFIDE (UNII: 44SIJ800OX) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRISULFIDE 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:71919-087-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/14/2010
2 NDC:71919-087-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/14/2010
3 NDC:71919-087-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/14/2010
4 NDC:71919-087-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/14/2010
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 12/14/2010
Labeler - Washington Homeopathic Products (084929389)
Establishment
Name Address ID/FEI Business Operations
Washington Homeopathic Products 084929389 manufacture(71919-087)

Revised: 12/2018
Document Id: 7e398bae-6f24-cdbd-e053-2a91aa0a0abb
Set id: 3d1e2518-152c-4a61-ba9c-f9fc07c1e681
Version: 2
Effective Time: 20181230
 
Washington Homeopathic Products