Label: BLUE CEDAR HAND SANITIZER- hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 55444-003-01 - Packager: Anhui Kiwi Biotech Co., Ltd.
- 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 April 26, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
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WARNINGS
Flammable. Keep away from fire or flame.
Forexternal use only.
Do not use this product in or near the eyes. In case of accidental contact, ninse eyes thoroughly with water.
Stop use and ask doctor if iritation or rash appears andlasts.
Keep away from children. If sallowed, get medicalhelp right away,
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLUE CEDAR HAND SANITIZER
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55444-003 Route of Administration EXTRACORPOREAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 150 mL in 200 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) .ALPHA.-TERPINEOL (UNII: 21334LVV8W) TERPINEOL (UNII: R53Q4ZWC99) .GAMMA.-NONALACTONE (UNII: I1XGH66S8P) LINALOOL, (+/-)- (UNII: D81QY6I88E) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) GLYCERETH-26 (UNII: NNE56F2N14) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) Product Characteristics Color Score Shape Size Flavor FRUIT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55444-003-01 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/21/2020 Labeler - Anhui Kiwi Biotech Co., Ltd. (554444636) Establishment Name Address ID/FEI Business Operations Anhui Kiwi Biotech Co., Ltd. 554444636 manufacture(55444-003)