NAT MUR 30C- natrum muriaticum liquid 
Energique, 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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DRUG FACTS:

ACTIVE INGREDIENT:

(in each drop) Natrum Muriaticum 30C 100%

PURPOSE:

Natrum Muriaticum - sneezing**

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

USES:

May temporarily relieve runny nose with watery discharge and much sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

Stop use and ask a doctor if symptoms persist for more than 7 days.

If pregnant or breast-feeding, 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.

• Do not use if tamper evident seal is broken or missing. • Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

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

DIRECTIONS:

• Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional.

• Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800-869-8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

NAT MUR 30C

1 fl. oz. (30 ml)

NAT MUR 30C

NAT MUR  30C
natrum muriaticum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0694
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0694-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/04/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/04/2024
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0694) , api manufacture(44911-0694) , label(44911-0694) , pack(44911-0694)

Revised: 1/2024
Document Id: 6ee5d857-7df6-4abf-8b23-e758bf978477
Set id: f23747a5-2420-43d3-b619-f1f1eaeae493
Version: 1
Effective Time: 20240104
 
Energique, Inc.