Label: DAWN ULTRA ANTIBACTERIAL HAND ORANGE SCENT- chloroxylenol soap
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NDC Code(s):
37000-617-10,
37000-617-11,
37000-617-12,
37000-617-16, view more37000-617-19, 37000-617-20, 37000-617-21, 37000-617-22, 37000-617-23, 37000-617-26, 37000-617-38, 37000-617-40, 37000-617-47, 37000-617-53, 37000-617-54, 37000-617-57, 37000-617-59, 37000-617-63, 37000-617-65, 37000-617-70, 37000-617-82
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 9, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.12L (1.18 QT) Bottle Label
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INGREDIENTS AND APPEARANCE
DAWN ULTRA ANTIBACTERIAL HAND ORANGE SCENT
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-617 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) DECETH-8 (UNII: 19FQ96EA8Q) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) PPG-26 (UNII: V86KZL3H2Z) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) SODIUM HYDROXIDE (UNII: 55X04QC32I) C9-11 PARETH-8 (UNII: 80E6PSE1XL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-617-26 266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 2 NDC:37000-617-59 591 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 3 NDC:37000-617-63 638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 12/12/2019 4 NDC:37000-617-70 709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 5 NDC:37000-617-10 1010 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 12/12/2019 6 NDC:37000-617-11 1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 7 NDC:37000-617-16 1660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 08/01/2024 8 NDC:37000-617-23 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 02/01/2021 9 NDC:37000-617-53 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 12/12/2019 10 NDC:37000-617-22 2210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 01/01/2022 11 NDC:37000-617-47 479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2018 12/01/2021 12 NDC:37000-617-57 573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2018 02/01/2025 13 NDC:37000-617-12 1210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2018 04/01/2021 14 NDC:37000-617-82 828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2018 15 NDC:37000-617-20 207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/2019 02/01/2024 16 NDC:37000-617-40 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/2019 12/01/2023 17 NDC:37000-617-19 192 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/30/2021 09/01/2024 18 NDC:37000-617-38 1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/30/2021 19 NDC:37000-617-21 221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2022 11/01/2025 20 NDC:37000-617-54 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 10/01/2025 21 NDC:37000-617-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 07/07/2014 Labeler - The Procter & Gamble Manufacturing Company (004238200)