Label: ACEVWER ITCH RELIEF- itch relief cream
- NDC Code(s): 83778-007-01
- Packager: Jiangxi Dentalbright Technology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 13, 2024
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- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
- Other information
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Inactive ingredients
Aqua, Allantoin, Beeswax, Borneol, Carbomer, C12-14 Pareth-7, Camellia Japonica Seed Oil, Cetyl Alcohol, Cnidium Monnieri Extract, Cyclohexasiloxane, Cyclopentamethylene Dimethylsiloxane, Glycerin, Glycerin Stearate, Hydrogenated Polyisobutene, Hydroxyacetophenone, Polysorbate-60, Polydimethylsiloxane, Polyacrylamide, Poria Cocos Sclerotium Extract, Sorbitan Stearate, Tocopherol Acetate, Trehalose, Triethanolamine, Xanthan Gum.
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INGREDIENTS AND APPEARANCE
ACEVWER ITCH RELIEF
itch relief creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83778-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVENA SATIVA (OAT) MEAL EXTRACT (UNII: 8PI54V663Y) (AVENA SATIVA (OAT) MEAL EXTRACT - UNII:8PI54V663Y) AVENA SATIVA (OAT) MEAL EXTRACT 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength C12-14 PARETH-7 (UNII: R66I1M1LNH) CYCLOHEXASILOXANE (UNII: XHK3U310BA) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE (UNII: 92RU3N3Y1O) ALLANTOIN (UNII: 344S277G0Z) TROLAMINE (UNII: 9O3K93S3TK) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN STEARATE (UNII: NVZ4I0H58X) BEESWAX (UNII: 2ZA36H0S2V) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) CARBOMER (UNII: 0A5MM307FC) POLYACRYLAMIDE (CROSSLINKED; 2 MOLE PERCENT BISACRYLAMIDE) (UNII: 9FPL31B58Q) WOLFIPORIA COCOS SCLEROTIUM (UNII: MTD53229ZC) BORNEOL (UNII: M89NIB437X) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) HYDROGENATED POLYISOBUTENE 8 (UNII: 7YR4ZFS62E) CAMELLIA JAPONICA SEED OIL (UNII: U37N0S910T) TREHALOSE (UNII: B8WCK70T7I) CNIDIUM MONNIERI FRUIT OIL (UNII: JK0MS9P8YL) GLYCERIN (UNII: PDC6A3C0OX) CYCLOMETHICONE (UNII: NMQ347994Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83778-007-01 50 g in 1 BOTTLE; Type 0: Not a Combination Product 11/12/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 11/12/2024 Labeler - Jiangxi Dentalbright Technology Co., Ltd (544503502) Establishment Name Address ID/FEI Business Operations Jiangxi Dentalbright Technology Co., Ltd 544503502 manufacture(83778-007)