Label: CHININUM SALICYLICUM pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 15631-0128-0, 15631-0128-1, 15631-0128-2, 15631-0128-3, view more15631-0128-4, 15631-0128-5 - Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- Category: HUMAN OTC DRUG LABEL
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 March 13, 2020
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- ACTIVE INGREDIENT
- USES
- INDICATIONS
- DOSAGE
- WARNINGS
- INACTIVE INGREDIENTS
- STORAGE
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QUESTIONS OR COMMENTS
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INGREDIENTS AND APPEARANCE
CHININUM SALICYLICUM
chininum salicylicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-0128 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUININE SALICYLATE (UNII: 6DY04L71DR) (SALICYLIC ACID - UNII:O414PZ4LPZ) QUININE SALICYLATE 3 [hp_X] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-0128-0 100 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 2 NDC:15631-0128-1 200 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 3 NDC:15631-0128-2 400 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 4 NDC:15631-0128-3 750 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 5 NDC:15631-0128-4 2500 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 6 NDC:15631-0128-5 12500 in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/02/2015 Labeler - Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994) Establishment Name Address ID/FEI Business Operations Rxhomeo Private Limited d.b.a. Rxhomeo, Inc 650833994 manufacture(15631-0128) , label(15631-0128)