Label: LEDUM PAL liquid
- NDC Code(s): 15631-2823-0, 15631-2823-1
- Packager: Rxhomeo Private Limited d.b.a. Rxhomeo, 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 June 5, 2024
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- ACTIVE INGREDIENT
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- INDICATIONS
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- INACTIVE INGREDIENTS
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INGREDIENTS AND APPEARANCE
LEDUM PAL
ledum pal liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:15631-2823 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) LEDUM PALUSTRE TWIG 1 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:15631-2823-0 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/23/2024 2 NDC:15631-2823-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/23/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/23/2024 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(15631-2823) , label(15631-2823)