NAT SULPH- sodium sulfate anhydrous tablet

NAT SULPH by

Drug Labeling and Warnings

NAT SULPH by is a Homeopathic medication manufactured, distributed, or labeled by Hyland's, Standard Homeopathic Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DIRECTIONS

Adults & Children ages 7 - 12: 4 tablets. Children ages 2 - 6: 2 tablets. Dissolve under tongue 3 times a day. Use more frequently (every 15 minutes for up to 8 doses) with acute conditions.

INDICATIONS

Relief of symptoms of the flu,nausea and vomiting.

FORMULA

Natrum Sulphuricum 30X HPUS

in a base of Acacia Gum, Lactose N.F.

“HPUS” indicates that the active ingredients are in the official Homeopathic Pharmacopœia of the United States.

Warnings

Do not use if imprinted cap band is broken or missing.

If symptoms persist for more than 7 days or worsen, contact a licensed health care provider.

Discontinue use if symptoms are accompanied by a high fever (over 101° F).

If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product.

Keep all medications out of the reach of children.

QUESTIONS?

(800) 624-9659

PRINCIPAL DISPLAY PANEL - 500 Tablet Bottle Label

HOMEOPATHIC

NDC: 54973-3111-1

Hyland's®

#11

Nat. Sulph. 30X

Flu Symptoms,

Nausea,Vomiting*

500 TABLETS

INGREDIENTS AND APPEARANCE

NAT SULPH 
sodium sulfate anhydrous tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54973-3111
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM SULFATE ANHYDROUS	30 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54973-3111-1	500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940
2	NDC: 54973-3111-2	1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940	12/31/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/1940

Labeler - Hyland's (028570695)

Establishment
Name	Address	ID/FEI	Business Operations
Standard Homeopathic Company		008316655	manufacture(54973-3111) , pack(54973-3111)