Label: RXHOMEO HOMEOPATHIC COMBO 3 kit
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Contains inactivated NDC Code(s)
NDC Code(s): 15631-2453-0 - Packager: Rxhomeo Private Limited d.b.a.
- 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 October 21, 2016
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- ACTIVE INGREDIENT
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USES
A homeopathic combination pack with two single remedies Badiaga and Kali Sulphuricum for treatment of dandruff.
Badiaga: Badiaga has marked action in treating dandruff. There is soreness of scalp with dry and tetter like dandruff. Pain in forehead and temple extending to eye balls with blueness under eyes.Kali Sulphuricum: Kali Sulph also helps in seborrhoea or dandruff and ringworm of scalp or beard with abundant scales. Sores on skin with thick, profuse, yellow watery secretion. Bald spots after gonorrhea.
- INDICATIONS
- DOSAGE
- WARNINGS
- INACTIVE INGREDIENTS
- STORAGE
- QUESTIONS OR COMMENTS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RXHOMEO HOMEOPATHIC COMBO 3
rxhomeo homeopathic combo 3 kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-2453 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-2453-0 1 in 1 CONTAINER 10/21/2016 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 Part 2 1 Part 1 of 2 BADIAGA
badiaga pelletProduct Information Item Code (Source) NDC:15631-0070 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SPONGILLA LACUSTRIS (UNII: 6SZ0G98BHM) (SPONGILLA LACUSTRIS - UNII:6SZ0G98BHM) SPONGILLA LACUSTRIS 2 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic Part 2 of 2 KALI SULPHURICUM
kali sulphuricum tabletProduct Information Item Code (Source) NDC:15631-0613 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE 1 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score no score Shape ROUND Size 3mm Flavor Imprint Code Contains Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/21/2016 Labeler - Rxhomeo Private Limited d.b.a. (650833994) Establishment Name Address ID/FEI Business Operations Rxhomeo Private Limited d.b.a.,Rxhomeo, Inc 650833994 manufacture(15631-2453) , label(15631-2453)
