Label: ERBIUM SULPHURICUM pellet
- NDC Code(s): 63545-699-01
- Packager: Hahnemann Laboratories, 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 July 27, 2022
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- Official Label (Printer Friendly)
- PATIENT MEDICATION INFORMATION
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- INDICATIONS & USAGE
- PURPOSE
- WARNINGS
- PREGNANCY OR BREAST FEEDING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- INSTRUCTIONS FOR USE
- DOSAGE & ADMINISTRATION
- ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
- Single label image contains content for sections 1-15.
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INGREDIENTS AND APPEARANCE
ERBIUM SULPHURICUM
erbium sulphuricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63545-699 Route of Administration BUCCAL, ORAL, SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ERBIUM SULFATE OCTAHYDRATE (UNII: 76R3969825) (ERBIUM - UNII:77B218D3YE) ERBIUM SULFATE OCTAHYDRATE 1 [hp_M] in 1 [hp_M] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color white Score no score Shape ROUND Size 2mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63545-699-01 730 [hp_M] in 1 VIAL, GLASS; Type 0: Not a Combination Product 07/09/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/09/2018 Labeler - Hahnemann Laboratories, Inc. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, Inc. 147098081 manufacture(63545-699)