Label: NO-GERMS HAND SANITIZER- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 79851-019-01, 79851-019-03, 79851-019-04, 79851-019-05, view more79851-019-06, 79851-019-07, 79851-019-08 - Packager: Millennium Research USA LLC
- 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 July 16, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
- 25 ml NDC 79851-019-01
- 4 L NDC 79851-019-05
- 50 ml NDC 79851-019-03
- 210 ml NDC 79851-019-09
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INGREDIENTS AND APPEARANCE
NO-GERMS HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79851-019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CITRIC ACID ACETATE (UNII: DSO12WL7AU) MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) LAVENDER OIL (UNII: ZBP1YXW0H8) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79851-019-08 24 in 1 CASE 08/26/2020 1 NDC:79851-019-07 12 in 1 CASE 1 NDC:79851-019-01 25 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 2 NDC:79851-019-06 12 in 1 CASE 08/26/2020 2 NDC:79851-019-03 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 3 NDC:79851-019-04 210 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/26/2020 4 NDC:79851-019-05 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/26/2020 Labeler - Millennium Research USA LLC (110101867) Establishment Name Address ID/FEI Business Operations Millennium Research Llc 110101867 manufacture(79851-019) , pack(79851-019) , label(79851-019)