Label: CARTILAGO ARGENTUM cream
- NDC Code(s): 48951-3260-5
- Packager: Uriel Pharmacy Inc.
- Category: HUMAN OTC DRUG LABEL
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 January 18, 2024
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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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. Contains traces of lactose. 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
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INGREDIENTS AND APPEARANCE
CARTILAGO ARGENTUM
cartilago argentum creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3260 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT 3 [hp_X] in 1 g ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 6 [hp_X] in 1 g ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X] in 1 g SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 8 [hp_X] in 1 g BOS TAURUS CARTILAGE (UNII: UE77B10IIY) (BOS TAURUS CARTILAGE - UNII:UE77B10IIY) BOS TAURUS CARTILAGE 8 [hp_X] in 1 g BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO) (BETULA PUBESCENS LEAF - UNII:84SOH0O3OO) BETULA PUBESCENS LEAF 3 [hp_X] in 1 g ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE 5 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) STEARIC ACID (UNII: 4ELV7Z65AP) FRANKINCENSE OIL (UNII: 67ZYA5T02K) WATER (UNII: 059QF0KO0R) SORBIC ACID (UNII: X045WJ989B) MYRRH OIL (UNII: H74221J5J4) LAVENDER OIL (UNII: ZBP1YXW0H8) CETYL ALCOHOL (UNII: 936JST6JCN) POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) XANTHAN GUM (UNII: TTV12P4NEE) TEA TREE OIL (UNII: VIF565UC2G) CITRUS PARADISI SEED (UNII: 12F08874Y7) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-3260-5 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(48951-3260)