Label: ELROSE LABS- conzerol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70223-001-06 - Packager: Elroselabs 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 December 17, 2015
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- WARNINGS
- ACTIVE INGREDIENT
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- PURPOSE
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
ELROSE LABS
conzerol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70223-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 6 mg in 28.3 mg OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 mg in 28.3 mg SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 6 [hp_X] in 28.3 mg POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 6 mg in 28.3 mg POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06) POTASSIUM BROMIDE 6 mg in 28.3 mg Inactive Ingredients Ingredient Name Strength CROTON LECHLERI WHOLE (UNII: 9K50DM06OR) WHITE WAX (UNII: 7G1J5DA97F) POLYSORBATE 60 (UNII: CAL22UVI4M) MAGNESIUM SULFATE (UNII: DE08037SAB) GLYCERIN (UNII: PDC6A3C0OX) Zinc Oxide (UNII: SOI2LOH54Z) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) TEA TREE OIL (UNII: VIF565UC2G) CLOVE OIL (UNII: 578389D6D0) METHYL SALICYLATE (UNII: LAV5U5022Y) OREGANO LEAF OIL (UNII: 7D0CGR40U1) LEMON BALM OIL (UNII: MJ76269K9S) JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G) NIAOULI OIL (UNII: D50IC2T8FU) EUCALYPTUS OIL (UNII: 2R04ONI662) COCONUT OIL (UNII: Q9L0O73W7L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70223-001-06 28.3 mg in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/16/2015 Labeler - Elroselabs Inc. (079977784) Establishment Name Address ID/FEI Business Operations Elroselabs Inc. 079977784 manufacture(70223-001)