Label: ARGENTYN 23- argentum metallicaum gel
- NDC Code(s): 52166-001-01, 52166-001-02, 52166-001-03
- Packager: Natural Immunogenics Corp.
- 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 20, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- 52166-001-01 59ML
- 52166-001-02 29ML
- 52166-001-03 5ML
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INGREDIENTS AND APPEARANCE
ARGENTYN 23
argentum metallicaum gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52166-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 30 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52166-001-01 1 in 1 BOX 01/01/2009 1 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:52166-001-02 1 in 1 BOX 01/01/2009 2 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:52166-001-03 5 mL in 1 POUCH; Type 0: Not a Combination Product 11/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2009 Labeler - Natural Immunogenics Corp. (048744085) Registrant - Natural Immunogenics Corp. (048744085)