Label: XPECT EXTRA STRENGTH ITCH RELIEF- diphenhydramine hydrochloride spray
- NDC Code(s): 42961-218-01
- Packager: Cintas Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use
- When using this produt
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
XPECT EXTRA STRENGTH ITCH RELIEF
diphenhydramine hydrochloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42961-218 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 2 mg in 100 mL Inactive Ingredients Ingredient Name Strength DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) C12-15 PARETH-9 (UNII: H3ZIY6WP1R) water (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42961-218-01 59.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/16/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/16/2022 Labeler - Cintas Corporation (056481716) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc 874965262 manufacture(42961-218)