Label: NUMIAN HERATAGE HAND SANITIZER- alcohol solution
- NDC Code(s): 64942-1756-1, 64942-1756-2
- Packager: Conopco, Inc. d/b/a/ Unilever
- 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 23, 2020
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- Official Label (Printer Friendly)
- Active Ingredient
- Use(s)
- Warnings
- Do not use
- WHEN USING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PACKAGE LABEL
-
INGREDIENTS AND APPEARANCE
NUMIAN HERATAGE HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1756 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 72 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Hydroxypropyl Cellulose, Unspecified (UNII: 9XZ8H6N6OH) Glycerin (UNII: PDC6A3C0OX) Apple (UNII: B423VGH5S9) Shea Butter (UNII: K49155WL9Y) Argan Oil (UNII: 4V59G5UW9X) Indian Frankincense (UNII: 4PW41QCO2M) Myrrh (UNII: JC71GJ1F3L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1756-1 95 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/10/2020 2 NDC:64942-1756-2 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/10/2020 Labeler - Conopco, Inc. d/b/a/ Unilever (001375088) Registrant - Apex International MFG, Inc. (015226132) Establishment Name Address ID/FEI Business Operations Apex International MFG, Inc. 015226132 manufacture(64942-1756)