Label: SULPHUR pellet
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NDC Code(s):
37662-2313-1,
37662-2313-2,
37662-2313-3,
37662-2314-1, view more37662-2314-2, 37662-2314-3, 37662-2315-1, 37662-2315-2, 37662-2315-3, 37662-2315-4, 37662-2316-1, 37662-2316-2, 37662-2316-3, 37662-2316-4, 37662-2317-1, 37662-2317-2, 37662-2317-3, 37662-2317-4, 37662-2318-1, 37662-2318-2, 37662-2318-3, 37662-2318-4, 37662-2319-1, 37662-2319-2, 37662-2319-3, 37662-2319-4, 37662-2320-1, 37662-2320-2, 37662-2320-3, 37662-2320-4, 37662-2321-1
- 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 January 11, 2023
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
SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2313 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2313-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2313-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2313-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2320 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2320-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2320-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2320-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2320-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2316 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2316-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2316-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2316-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2316-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2317 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2317-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2317-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2317-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2317-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2318 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2318-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2318-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2318-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2318-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2319 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2319-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2319-2 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2319-3 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2319-4 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2321 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2321-1 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2314 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2314-1 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2314-2 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2314-3 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 SULPHUR
sulphur pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37662-2315 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 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:37662-2315-1 80 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 2 NDC:37662-2315-2 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 01/11/2023 3 NDC:37662-2315-3 1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 4 NDC:37662-2315-4 4000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/11/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/11/2023 Labeler - Hahnemann Laboratories, INC. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, INC. 147098081 manufacture(37662-2313, 37662-2314, 37662-2315, 37662-2316, 37662-2317, 37662-2318, 37662-2319, 37662-2320, 37662-2321)
