Label: ALOE TOUCH- hand sanitizer liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71020-010-02 - Packager: Sante Manufacturing Inc
- Category: HUMAN OTC DRUG LABEL
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 March 10, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- INSTRUCTIONS FOR USE
- OTHER SAFETY INFORMATION
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALOE TOUCH
hand sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71020-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 700 mL in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER 940 (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71020-010-02 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/10/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/10/2017 Labeler - Sante Manufacturing Inc (242048747) Establishment Name Address ID/FEI Business Operations Sante Manufacturing Inc. 242048747 manufacture(71020-010)