Label: HERMON MOLLUSCUM CONTAGIOSUM TREATMENT OIL- molluscum contagiosum treatment oil
HERMON MOLLUSCUM CONTAGIOSUM TREATMENT OIL- tea tree oil body wash oil
- NDC Code(s): 82739-006-01, 82739-007-01
- Packager: Shenzhen Situya Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 6, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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Active Ingredient
15ML:
SILVER NITRATE 10%
ECHINACEAANGUSTIFOLIA WHOLE 10%
FUCUS VESICULOSUS 5%
THUJA OCCIDENTALIS BARK 5%
TEATREE OIL.50%
MENTHOL,UNSPECIFIED FORM 0.50%60ML:
SODIUM COCOYL GLUTAMATE10%
POTASSIUM COCOYL GLYCINATE 5%
SODIUM LAUROYL SARCOSINATE 5%
SODIUM METHYL COCOYL TAURATE 3%
SODIUM LAURETH-3 SULFATE 2%
SODIUM LAURYL SULFATE 2% - Purpose
- Use
- Warnings
- Do not use
- STOP USE section
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
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Directions
Use Hermon Body Wash 5day. Wash affected areas and dry thoroughly. Applythe product 3 to 4 times daily to the affected area using the brush applicator. Allowto dry completely. Over the next 1 to 2 weeks, Molluscum warts will start toredden and scab over. Molluscum papules will then diminish, dry up and flakeaway over a 2-6 weeks period.
- Inactive ingredients
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HERMON MOLLUSCUM CONTAGIOSUM TREATMENT OIL
molluscum contagiosum treatment oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82739-006 Route of Administration EXTRACORPOREAL, CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THUJA OCCIDENTALIS BARK (UNII: 19RAD88E6O) (THUJA OCCIDENTALIS BARK - UNII:19RAD88E6O) THUJA OCCIDENTALIS BARK 5 g in 100 mL TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G) TEA TREE OIL 0.5 g in 100 mL ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 10 g in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.5 g in 100 mL FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 5 g in 100 mL SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION 10 g in 100 mL CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82739-006-01 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/05/2023 HERMON MOLLUSCUM CONTAGIOSUM TREATMENT OIL
tea tree oil body wash oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82739-007 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCO MONOETHANOLAMIDE (UNII: C80684146D) (COCO MONOETHANOLAMIDE - UNII:C80684146D) COCO MONOETHANOLAMIDE 0.5 g in 100 mL COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) (COCAMIDOPROPYL BETAINE - UNII:5OCF3O11KX) COCAMIDOPROPYL BETAINE 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) GLYCERIN (UNII: PDC6A3C0OX) TEA TREE OIL (UNII: VIF565UC2G) WATER (UNII: 059QF0KO0R) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) PAEONIA SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) LAURYL SULFATE (UNII: DIQ16UC154) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) PURSLANE (UNII: M6S840WXG5) CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0) OPUNTIA STREPTACANTHA STEM (UNII: 3TF9Z1U73O) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) POTASSIUM COCOYL GLYCINATE (UNII: WZ70FUF22U) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) SODIUM CHLORIDE (UNII: 451W47IQ8X) PANTHENOL (UNII: WV9CM0O67Z) TOCOPHEROL (UNII: R0ZB2556P8) LEVOMENOL (UNII: 24WE03BX2T) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82739-007-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/05/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/05/2023 Labeler - Shenzhen Situya Trading Co., Ltd. (706154255) Establishment Name Address ID/FEI Business Operations Shenzhen Situya Trading Co., Ltd. 706154255 manufacture(82739-006, 82739-007)