Label: 75% ALCOHOL INSTANT HAND SANITIZER gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75242-007-01, 75242-007-02, 75242-007-03, 75242-007-04, view more75242-007-05, 75242-007-06, 75242-007-07, 75242-007-08, 75242-007-09, 75242-007-10, 75242-007-11, 75242-007-12, 75242-007-13, 75242-007-14, 75242-007-15, 75242-007-16 - Packager: Cannapresso Health. 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 May 20, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- package label
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INGREDIENTS AND APPEARANCE
75% ALCOHOL INSTANT HAND SANITIZER
75% alcohol instant hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75242-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength LAVENDER OIL (UNII: ZBP1YXW0H8) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75242-007-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 2 NDC:75242-007-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 3 NDC:75242-007-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 4 NDC:75242-007-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 5 NDC:75242-007-05 119 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 6 NDC:75242-007-06 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 7 NDC:75242-007-07 149 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 8 NDC:75242-007-08 199 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 9 NDC:75242-007-09 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 10 NDC:75242-007-10 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 11 NDC:75242-007-11 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 12 NDC:75242-007-12 349 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 13 NDC:75242-007-13 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 14 NDC:75242-007-14 499 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 15 NDC:75242-007-15 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 16 NDC:75242-007-16 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - Cannapresso Health. Inc. (117477763) Establishment Name Address ID/FEI Business Operations Cannapresso Health. Inc. 117477763 manufacture(75242-007)
