Label: ACHYRANTHES CALEA pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-6441-1 - Packager: HOMEOLAB USA 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 12, 2017
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- ACTIVE INGREDIENT HPUS
- PURPOSE
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- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS?
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INGREDIENTS AND APPEARANCE
ACHYRANTHES CALEA
achyranthes calea pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6441 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IRESINE CALEA (UNII: O8F89913OT) (IRESINE CALEA - UNII:O8F89913OT) IRESINE CALEA 1 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60512-6441-1 80 in 1 TUBE; Type 0: Not a Combination Product 05/31/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/11/1995 Labeler - HOMEOLAB USA INC. (202032533) Registrant - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-6441)