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
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 23, 2023
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- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- 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 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 not final part333E 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)