Label: BATINHA 40 (NUMBER 532)- hypericum peltatum, arsenicum album pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 69152-0532-1 - Packager: Paramesh Banerji Life Sciences LLC
- 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 July 30, 2018
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- DRUG FACTS: Active Ingredients
- Inactive Ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children
- Direction
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Manufactured by
Paramesh Banerji Life Sciences, LLC.
North Brunswick, NJ 08902, USA.
Tel: +1-732-743-5936
Email: info@pblifesciences.com
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INGREDIENTS AND APPEARANCE
BATINHA 40 (NUMBER 532)
hypericum peltatum, arsenicum album pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69152-0532 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 30 [hp_C] KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (KALMIA LATIFOLIA LEAF - UNII:79N6542N18) KALMIA LATIFOLIA LEAF 6 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) Product Characteristics Color white Score Shape ROUND Size 4mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69152-0532-1 96 in 1 BOTTLE; Type 0: Not a Combination Product 07/30/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/10/2014 Labeler - Paramesh Banerji Life Sciences LLC (079393726) Establishment Name Address ID/FEI Business Operations Paramesh Banerji Life Sciences LLC 079393726 pack(69152-0532) , manufacture(69152-0532) , label(69152-0532)