Label: EOS MEDICATED PAIN RELIEF COLD SORE TREATMENT- allantoin, camphor, menthol ointment
- NDC Code(s): 70170-0023-1
- Packager: eos Products LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 25, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
-
Inactive Ingredients:
Bis-Diglyceryl Polyacyladipate-2, Jojoba Esters, Hydrogenated Polyisobutene, Ricinus Communis (Castor) Seed Oil, Dimer Dilinoleyl Dimer Dilinoleate, Diisostearyl Malate, Octyldodecanol, Nylon-12, Beeswax/Cire d'abeille, Helianthus Annuus (Sunflower) Seed Wax, Flavor/Aroma, Silica Dimethyl Silylate, Theobroma Cacao (Cocoa) Seed Butter, Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Polyglycerin-3, Acacia Decurrens Flower Wax, Stearalkonium Hectorite, Stevia Rebaudiana Leaf/Stem Extract, Helianthus Annuus (Sunflower) Seed Oil, Propylene Carbonate, Limonene, Mentha Piperita (Peppermint) Leaf Extract, Linalool, Tocopherol, Citric Acid.
- Questions or comments?
- Principal Display Panel 0.35 fl. oz. (10mL)
-
INGREDIENTS AND APPEARANCE
EOS MEDICATED PAIN RELIEF COLD SORE TREATMENT
allantoin, camphor, menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70170-0023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.0575 g in 10 mL CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.046 g in 10 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.046 g in 10 mL Inactive Ingredients Ingredient Name Strength FRAGRANCE PEPPERMINT ORC2000647 (UNII: UHZ8T78D8B) OCTYLDODECANOL (UNII: 461N1O614Y) HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) COCOA BUTTER (UNII: 512OYT1CRR) SUNFLOWER OIL (UNII: 3W1JG795YI) ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) PROPYLENE CARBONATE (UNII: 8D08K3S51E) BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T) NYLON-12 (UNII: 446U8J075B) CASTOR OIL (UNII: D5340Y2I9G) YELLOW WAX (UNII: 2ZA36H0S2V) LINALOOL, (+/-)- (UNII: D81QY6I88E) DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ) SHEA BUTTER (UNII: K49155WL9Y) MENTHA PIPERITA LEAF (UNII: A389O33LX6) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LIMONENE, (+)- (UNII: GFD7C86Q1W) DIMER DILINOLEYL DIMER DILINOLEATE (UNII: 0E2D5DBT7M) TOCOPHEROL (UNII: R0ZB2556P8) STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876) HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70170-0023-1 1 in 1 BLISTER PACK 11/01/2023 1 10 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 11/01/2023 Labeler - eos Products LLC (803969620)