Label: ANTIBACTERIAL HAND WASH SPRING RAIN- benzalkonium chloride soap
- NDC Code(s): 83986-012-32
- Packager: UpLift Brands, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 9, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
-
Inactive Ingredients
water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, glycerin, myristamidopropylamine oxide, fragrance, hexyl cinnamal, linalool, limonene, disteareth-75 IPDI, PEG-150 distearate, citric acid, sodium chloride, tetrasodium EDTA, benzophenone-4, sodium benzoate, ext. violet 2, green 3
- Adverse reaction
- Principal panel display
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL HAND WASH SPRING RAIN
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83986-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength EDETATE SODIUM (UNII: MP1J8420LU) SULISOBENZONE (UNII: 1W6L629B4K) WATER (UNII: 059QF0KO0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) GLYCERIN (UNII: PDC6A3C0OX) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM BENZOATE (UNII: OJ245FE5EU) EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83986-012-32 355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/12/2022 Labeler - UpLift Brands, LLC (119091527) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(83986-012) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(83986-012)