Label: SILVAPLEX WOUND- argentum metallicum spray
- NDC Code(s): 72363-015-01
- Packager: AG Essence
- 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 November 16, 2023
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- Official Label (Printer Friendly)
- DIRECTIONS FOR USE
- WARNING
- Precaution:
- Ingredients
- Ingredients
- Homeopathic Wound Spray
- Indications for Use
- WARNING:
- SilvaPlex Wound Spray
- SilvaPlex Wound Spray
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INGREDIENTS AND APPEARANCE
SILVAPLEX WOUND
argentum metallicum sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72363-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 0.047 g in 236 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 231.468 g in 236 g CHITOSAN LOW MOLECULAR WEIGHT (20-200 MPA.S) (UNII: SBD1A2I75N) 0.937 g in 236 g ARGININE (UNII: 94ZLA3W45F) 0.944 g in 236 g ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 0.234 g in 236 g GLYCERIN (UNII: PDC6A3C0OX) 2.37 g in 236 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72363-015-01 236 g in 1 BOTTLE; Type 0: Not a Combination Product 12/06/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/06/2023 Labeler - AG Essence (068562165) Registrant - AG Essence (068562165) Establishment Name Address ID/FEI Business Operations AG Essence 068562165 manufacture(72363-015)
