NATRUM MURIATICUM- sodium chloride granule 
Seroyal USA

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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NATRUM MURIATICUM

Active Ingredient

NATRUM MURIATICUM (Sodium chloride) 12CH GR

NATRUM MURIATICUM (Sodium chloride) 15CH GR

NATRUM MURIATICUM (Sodium chloride) 200CH GR

NATRUM MURIATICUM (Sodium chloride) 200K GR

NATRUM MURIATICUM (Sodium chloride) 30CH GR

NATRUM MURIATICUM (Sodium chloride) 30K GR

NATRUM MURIATICUM (Sodium chloride) 5CH GR

NATRUM MURIATICUM (Sodium chloride) 6CH GR

NATRUM MURIATICUM (Sodium chloride) 9CH GR

NATRUM MURIATICUM (Sodium chloride) CMK GR

NATRUM MURIATICUM (Sodium chloride) XMK GR

Indications

For the temporary relief of symptoms associated
with cold and flu

Warning

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children.

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

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children.

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

Inactive Ingredients

Lactose,

sucrose.

Directions

Adults: Take five granules three times daily or as recommended by your healthcare practitioner.

Children: Take three granules and follow adult directions.

QUESTIONS? 1-888-737-6925.

Indications

For the temporary relief of symptoms associated
with cold and flu

Directions

Adults: Take five granules three times daily or as recommended by your healthcare practitioner.

Children: Take three granules and follow adult directions.

62106-5206

UNDA

Do not use if label perforation is broken

Homeopathic Remedy

NDC : 62106-5206-4

NATRUM MURIATICUM

Sodium chloride

140 granules

Indications

For the temporary relief of symptoms associated
with cold and flu

NATRUM MURIATICUM 
sodium chloride granule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-5206
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE1 [hp_X]
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62106-5206-410 in 1 CARTON01/29/201508/31/2024
1140 in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/29/201508/31/2024
Labeler - Seroyal USA (018361118)
Establishment
NameAddressID/FEIBusiness Operations
SAN’UP401010287manufacture(62106-5206)

Revised: 10/2023
Document Id: 075fbe4d-5b80-f1ab-e063-6294a90adec8
Set id: 0dce7b9f-a284-700c-e054-00144ff88e88
Version: 4
Effective Time: 20231010
 
Seroyal USA