Label: ARGENTUM MALACHITE cream
- NDC Code(s): 48951-1309-5
- Packager: Uriel Pharmacy 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 February 12, 2024
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- Official Label (Printer Friendly)
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Spring water, Organic vinegar, Stearic acid, Glycerin, Isopropyl myristate, Lavender oil, Mineral oil, Povidone-iodine, Rosemary oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Myrrh oil, Grapefruit seed extract
"prepared using rhythmical processes"
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARGENTUM MALACHITE
argentum malachite creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-1309 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUPRIC CATION (UNII: 8CBV67279L) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION 3 [hp_X] in 1 g MERCURY (UNII: FXS1BY2PGL) (MERCURY - UNII:FXS1BY2PGL) MERCURY 6 [hp_X] in 1 g SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 3 [hp_X] in 1 g AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM) (AZADIRACHTA INDICA FLOWER - UNII:3TE8A92UPM) AZADIRACHTA INDICA FLOWER 2 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength LAVENDER OIL (UNII: ZBP1YXW0H8) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POVIDONE-IODINE (UNII: 85H0HZU99M) ROSEMARY OIL (UNII: 8LGU7VM393) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) SORBIC ACID (UNII: X045WJ989B) TEA TREE OIL (UNII: VIF565UC2G) POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I) XANTHAN GUM (UNII: TTV12P4NEE) FRANKINCENSE OIL (UNII: 67ZYA5T02K) MYRRH OIL (UNII: H74221J5J4) CITRUS PARADISI SEED (UNII: 12F08874Y7) ACETIC ACID (UNII: Q40Q9N063P) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-1309-5 60 g in 1 TUBE; Type 0: Not a Combination Product 09/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-1309)
