Label: DAWN ULTRA ANTIBACTERIAL HAND APPLE BLOSSOM SCENT- chloroxylenol soap
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NDC Code(s):
37000-616-01,
37000-616-02,
37000-616-03,
37000-616-04, view more37000-616-05, 37000-616-10, 37000-616-11, 37000-616-12, 37000-616-16, 37000-616-17, 37000-616-19, 37000-616-20, 37000-616-21, 37000-616-22, 37000-616-23, 37000-616-24, 37000-616-38, 37000-616-40, 37000-616-41, 37000-616-43, 37000-616-44, 37000-616-45, 37000-616-47, 37000-616-53, 37000-616-54, 37000-616-57, 37000-616-59, 37000-616-63, 37000-616-65, 37000-616-70, 37000-616-71, 37000-616-82, 37000-616-88, 37000-616-90
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 8, 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
- Use
- Warnings
- Directions
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 532 mL (1.12PT) 18 FL OZ Bottle Label
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INGREDIENTS AND APPEARANCE
DAWN ULTRA ANTIBACTERIAL HAND APPLE BLOSSOM SCENT
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-616 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 C9-11 PARETH-8 (UNII: 80E6PSE1XL) ALCOHOL (UNII: 3K9958V90M) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) PPG-26 (UNII: V86KZL3H2Z) DECETH-8 (UNII: 19FQ96EA8Q) SODIUM HYDROXIDE (UNII: 55X04QC32I) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-616-41 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 2 NDC:37000-616-59 591 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 3 NDC:37000-616-63 638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 4 NDC:37000-616-70 709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 5 NDC:37000-616-82 828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 6 NDC:37000-616-88 887 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 7 NDC:37000-616-10 1010 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 12/12/2019 8 NDC:37000-616-11 1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 01/10/2018 9 NDC:37000-616-16 1660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 10 NDC:37000-616-90 2660 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/07/2014 11 NDC:37000-616-22 2210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 02/06/2025 12 NDC:37000-616-23 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 09/01/2024 13 NDC:37000-616-43 431 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 12/12/2019 14 NDC:37000-616-53 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/10/2017 12/12/2019 15 NDC:37000-616-01 2 in 1 PACKAGE 02/10/2017 12/12/2019 15 638 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 16 NDC:37000-616-02 2 in 1 PACKAGE 02/10/2017 12/12/2019 16 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 17 NDC:37000-616-03 2 in 1 PACKAGE 03/28/2018 12/31/2021 17 828 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 18 NDC:37000-616-04 2 in 1 PACKAGE 03/28/2018 02/01/2021 18 573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 19 NDC:37000-616-12 1210 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/06/2018 02/01/2021 20 NDC:37000-616-47 479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/06/2018 12/01/2023 21 NDC:37000-616-57 573 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/06/2018 02/01/2025 22 NDC:37000-616-20 207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2019 02/01/2024 23 NDC:37000-616-40 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2019 01/01/2024 24 NDC:37000-616-71 709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/02/2019 12/01/2023 25 NDC:37000-616-19 192 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/30/2021 08/01/2024 26 NDC:37000-616-45 458 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/18/2021 27 NDC:37000-616-38 1120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/18/2021 28 NDC:37000-616-21 221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2022 02/01/2025 29 NDC:37000-616-54 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 30 NDC:37000-616-24 2070 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 31 NDC:37000-616-44 434 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 32 NDC:37000-616-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/07/2023 33 NDC:37000-616-05 3 in 1 CELLO PACK 02/07/2023 33 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 34 NDC:37000-616-17 171 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2024 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)
