Label: NATRUM MURIATICUM spray
- NDC Code(s): 71753-8009-1
- Packager: Ratis, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated January 20, 2022
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- ACTIVE INGREDIENT:
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USES:
Helps relieve conditions with excess water or dryness such as runny or stuffy nose, allergies, headaches, migraines, constipation, slow digestion, watery eyes, and dry mouth.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
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INDICATIONS:
Helps relieve conditions with excess water or dryness such as runny or stuffy nose, allergies, headaches, migraines, constipation, slow digestion, watery eyes, and dry mouth.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
NATRUM MURIATICUM
natrum muriaticum sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71753-8009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71753-8009-1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/30/2020 10/26/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/30/2020 10/26/2025 Labeler - Ratis, LLC (964594324)
