Label: NATRUM MURIATICUM pellet
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NDC Code(s):
37662-1878-1,
37662-1878-2,
37662-1878-3,
37662-1879-1, view more37662-1879-2, 37662-1879-3, 37662-1880-1, 37662-1880-2, 37662-1880-3, 37662-1880-4, 37662-1881-1, 37662-1881-2, 37662-1881-3, 37662-1881-4, 37662-1882-1, 37662-1882-2, 37662-1882-3, 37662-1882-4, 37662-1883-1, 37662-1883-2, 37662-1883-3, 37662-1883-4, 37662-1884-1, 37662-1884-2, 37662-1884-3, 37662-1884-4, 37662-1885-1, 37662-1885-2, 37662-1885-3, 37662-1885-4, 37662-1886-1
- Packager: Hahnemann Laboratories, INC.
- 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 November 8, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1880 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 30 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1880-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1880-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1880-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1880-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1879 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 12 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1879-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1879-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1879-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1882 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1882-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1882-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1882-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1882-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1886 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 1 [hp_Q] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 1mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1886-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1881 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 100 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1881-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1881-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1881-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1881-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1885 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 10 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1885-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1885-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1885-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1885-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1883 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 500 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1883-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1883-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1883-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1883-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1878 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1878-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1878-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1878-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 NATRUM MURIATICUM
natrum muriaticum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-1884 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37662-1884-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 2 NDC:37662-1884-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 11/08/2022 3 NDC:37662-1884-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 4 NDC:37662-1884-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2022 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-1878, 37662-1879, 37662-1880, 37662-1881, 37662-1882, 37662-1883, 37662-1884, 37662-1885, 37662-1886)
