Wild Yam Ginger by Uriel Pharmacy Inc WILD YAM GINGER spray

Wild Yam Ginger by

Drug Labeling and Warnings

Wild Yam Ginger by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: ONLY FOR USE AS A NASAL SPRAY.

DOSAGE & ADMINISTRATION

Use before bedtime. Ages 12 and older: 1-2 sprays. Ages 2-11: 1 spray. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Dioscorea villosa (Wild yam) 2X, Zingiberis (Ginger) 2X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Sodium chloride, Grapefruit seed extract

Prepared using rhythmical processes.

PURPOSE

Use: Temporary relief of snoring.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.
SHAKE WELL BEFORE USE.
REFRIGERATE AFTER OPENING.
USE WITHIN 30 DAYS OF OPENING.

QUESTIONS

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WILD YAM GINGER 
wild yam ginger spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-9283
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (DIOSCOREA VILLOSA ROOT - UNII:IWY3IWX2G8)	DIOSCOREA VILLOSA ROOT	2 [hp_X]  in 1 mL
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	2 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRUS PARADISI SEED (UNII: 12F08874Y7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-9283-2	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc		043471163	manufacture(48951-9283)