NATRUM SULPHURICUM- natrum sulphuricum spray 
Ratis, LLC

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 INGREDIENT:

Natrum Sulphuricum 6X.

USES:

Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults: 2 sprays 3 times a day or as needed.

Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

INDICATIONS:

Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized Water, Organic Ethanol 20%

QUESTIONS:

Comments? Visit

HomeopathyStore.com

or call (888) 405-7551.

Distributed by:

Ratis, LLC,

211 E. Lombard St, STE 303,

Baltimore, MD 21202

PACKAGE LABEL DISPLAY:

NDC 71753-8011-1

LACTOSE FREE

Anna's

REMEDIES

NATRUM SULPHURICUM

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

NATRUM SULPHURICUM

NATRUM SULPHURICUM 
natrum sulphuricum spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-8011
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71753-8011-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/30/202010/26/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/30/202010/26/2025
Labeler - Ratis, LLC (964594324)

Revised: 1/2022
Document Id: 2cc44cf3-5cfb-4a35-a8ea-06831753548a
Set id: ca0e0398-3e97-4e6c-a419-cdfb6f85bce6
Version: 2
Effective Time: 20220120
 
Ratis, LLC