Label: SILVAPLEX WOUND GEL- wound gel gel
- NDC Code(s): 72363-012-04
- 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 September 18, 2023
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- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
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INDICATIONS & USAGE
Indications for use: for relief of these symptoms due to minor Wounds,burns, Scrapes, Ulcerations or Minor Infections, Burning, Stinging, Itching, Redness, Minor Pain and Minor Inflammation.*
*These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat cure or prevent any disease.
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INGREDIENTS AND APPEARANCE
SILVAPLEX WOUND GEL
wound gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72363-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 5.9 g in 118 g Inactive Ingredients Ingredient Name Strength POLYQUATERNIUM-4 (1600 MPA.S AT 2%) (UNII: YE8J8372VI) 8.85 g in 118 g ARGININE (UNII: 94ZLA3W45F) 2.36 g in 118 g WATER (UNII: 059QF0KO0R) 89.916 g in 118 g GLYCERIN (UNII: PDC6A3C0OX) 10.974 g in 118 g Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72363-012-04 118 g in 1 JAR; Type 0: Not a Combination Product 03/24/2022 03/24/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/24/2022 03/24/2025 Labeler - AG Essence (068562165) Registrant - AG Essence Inc. (068562165) Establishment Name Address ID/FEI Business Operations AG Essence 068562165 manufacture(72363-012)