Label: ERON HEALING TONIC- zinc pyrithione shampoo
- NDC Code(s): 61558-100-01, 61558-100-03
- Packager: Geumseong TK
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 21, 2023
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- Official Label (Printer Friendly)
- Active Ingredient PurposePanthenol (0.5%) --------------Scalp Care Pyrithione Zinc (0.6%)---Anti-dandruff
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INACTIVE INGREDIENT
Inactive Ingredients
Sodium Laureth Sulfate, Water, Pueraria Lobata Root Extract,Pinus Densiflora Leaf Extract, Ginkgo Biloba Leaf Extract, Artemisia Princeps Leaf Extract,Cnidium Officinale Root Extract, Ammonium Lauryl Sulfate, TEA-Lauryl Sulfate, Disodium laureth sulfosuccinate, Cocamidopropyl Betaine, Polyquaternium-7, Butylene Glycol, Sodium Chloride, Propylene Glycol, Sodium PC, Tetrasodium EDTA, Perfume, Salicylic Acid, Disodium EDTA, Polyquaternium-10, Menthol, Methyl Paraben, Camellia Sinensis Leaf Extract, Methylchloroisothiazolinone, Methylisothiazolinone, Caramel
- PURPOSE
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For external use only
Do not use when
§ Your scalp is red, inflamed, irritated or painful.
When using this product
Do not apply on other parts of the body. Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not apply directly to wound or open cut. Stop use and ask doctor if rash or irritation on scalp develops and lasts. Do not swallow. In case of accidental ingestion, seek professional assistance. Store at room temperature.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- Eron Healing Tonic
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INGREDIENTS AND APPEARANCE
ERON HEALING TONIC
zinc pyrithione shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61558-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 3 g in 500 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 2.5 g in 500 mL Inactive Ingredients Ingredient Name Strength SODIUM LAURETH SULFATE (UNII: BPV390UAP0) WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM CHLORIDE (UNII: 451W47IQ8X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) EDETATE SODIUM (UNII: MP1J8420LU) SALICYLIC ACID (UNII: O414PZ4LPZ) EDETATE DISODIUM (UNII: 7FLD91C86K) MENTHOL (UNII: L7T10EIP3A) METHYLPARABEN (UNII: A2I8C7HI9T) GREEN TEA LEAF (UNII: W2ZU1RY8B0) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) CARAMEL (UNII: T9D99G2B1R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61558-100-03 1 in 1 CARTON 08/12/2019 1 NDC:61558-100-01 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/30/2013 Labeler - Geumseong TK (557821942) Registrant - Geumseong TK (557821942) Establishment Name Address ID/FEI Business Operations Geumseong TK 557821942 manufacture(61558-100)