Label: HAND SANITIZER GEL gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72449-101-01, 72449-101-02 - Packager: LS Promotions 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 16, 2020
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- Drug Facts
- Active Ingredient
- PURPOSE
- USES
- WARNINGS
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS?
- PDP_ Packet
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INGREDIENTS AND APPEARANCE
HAND SANITIZER GEL
hand sanitizer gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72449-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 mL in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER 1342 (UNII: 809Y72KV36) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72449-101-01 2.9 mL in 1 PACKET; Type 0: Not a Combination Product 03/16/2020 2 NDC:72449-101-02 5.9 mL in 1 PACKET; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/16/2020 Labeler - LS Promotions Inc. (024818391) Registrant - LS Promotions Inc. (024818391) Establishment Name Address ID/FEI Business Operations LS Promotions Inc. 024818391 manufacture(72449-101)