NATRUM SULPHURICUM- natrum sulphuricum pellet 
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc

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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ACTIVE INGREDIENT

NATRUM SULPHURICUM HPUS 1X and higher

USES

USES: Temporary Relief - Nasal Congestion*

* Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS

Condition listed above or as directed by the physician

DOSAGE

Adults- Take 4 or 6 Pellets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.

WARNINGS

This product is to be used for self-limiting conditions

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product

Keep this and all medication out of reach of children

INACTIVE INGREDIENTS

Sucrose

STORAGE

Store in a cool dark place

QUESTIONS OR COMMENTS

www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

Rxhomeo, Inc 3200 Commander Dr, Ste 100-W1, Carrollton, TX 75006 USA

Mini-Label

Label-Pellets

Blister-label

carton-label

NATRUM SULPHURICUM 
natrum sulphuricum pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15631-0312
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE1 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:15631-0312-0100 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
2NDC:15631-0312-1200 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
3NDC:15631-0312-2400 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
4NDC:15631-0312-3750 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
5NDC:15631-0312-42500 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
6NDC:15631-0312-512500 in 1 PACKAGE; Type 0: Not a Combination Product01/01/2018
7NDC:15631-0312-6500 in 1 PACKAGE; Type 0: Not a Combination Product08/23/2021
8NDC:15631-0312-71000 in 1 PACKAGE; Type 0: Not a Combination Product08/23/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/11/2015
Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994)
Establishment
NameAddressID/FEIBusiness Operations
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc650833994manufacture(15631-0312) , label(15631-0312)

Revised: 10/2021
Document Id: cdb3000d-50e7-d6ac-e053-2995a90a7312
Set id: d4e87869-f21c-4324-97f4-d4b52ba12fd3
Version: 4
Effective Time: 20211006
 
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc