Label: ALCARE EXTRA HAND SANITIZER- alcohol solution
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NDC Code(s):
11084-006-01,
11084-006-12,
11084-006-27,
11084-006-40, view more11084-006-66
- Packager: SC Johnson Professional USA, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Active ingredient
- Purpose
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- Inactive ingredients
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PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label
SCJ PROFESSIONAL
HEALTHCAREAlcare®
NDC 11084-006-27
Hand Sanitizer
Foaming Antiseptic Handrub
ExtraExcellent Moisturization
15
seconds
Fast-acting
CHG CompatibleSC Johnson Professional USA, Inc.
Charlotte, NC 28217
1-866-783-0422
Pat. www.scjp.com/patents
www.scjp.com
Made in Canada1 Liter (33.8 fl oz)
SAP # 400000076
L-1398 R0REORDER #
101561deb
SKIN CAREOpen for
Drug Facts -
INGREDIENTS AND APPEARANCE
ALCARE EXTRA HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) COCO-GLUCOSIDE (UNII: ICS790225B) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERYL OLEATE (UNII: 4PC054V79P) PANTHENOL (UNII: WV9CM0O67Z) PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-006-01 47 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2017 2 NDC:11084-006-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2017 3 NDC:11084-006-27 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2017 12/31/2026 4 NDC:11084-006-12 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2017 5 NDC:11084-006-66 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/17/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug 505G(a)(3) 03/01/2017 Labeler - SC Johnson Professional USA, Inc. (607378015) Registrant - SC Johnson Professional USA, Inc. (078805627) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 manufacture(11084-006)