Label: AMMONIUM CARBONICUM pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 63545-943-01, 63545-943-02, 63545-943-03, 63545-943-04 - Packager: Hahnemann Laboratories, 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 October 6, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- DOSAGE FORMS & STRENGTHS
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- 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
- STOP USE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AMMONIUM CARBONICUM
ammonium carbonicum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63545-943 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (CARBONATE ION - UNII:7UJQ5OPE7D) AMMONIUM CARBONATE 200 [hp_C] 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:63545-943-01 200 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/06/2020 2 NDC:63545-943-02 500 in 1 VIAL, GLASS; Type 0: Not a Combination Product 10/06/2020 3 NDC:63545-943-03 3000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/06/2020 4 NDC:63545-943-04 10000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/06/2020 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/06/2020 Labeler - Hahnemann Laboratories, Inc. (147098081) Registrant - Hahnemann Laboratories, Inc. (147098081) Establishment Name Address ID/FEI Business Operations Hahnemann Laboratories, Inc. 147098081 manufacture(63545-943)
