Label: KORA DAILY SAFE 70- hand sanitizer gel gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75504-170-11 - Packager: Kora Holdings LLC
- 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 December 15, 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
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WHEN USING
When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation, swelling or redness develops.
Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KORA DAILY SAFE 70
hand sanitizer gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75504-170 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 26.8 mL in 100 mL HYALURONATE SODIUM (UNII: YSE9PPT4TH) 0.1 mL in 100 mL CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) 0.3 mL in 100 mL TROLAMINE (UNII: 9O3K93S3TK) 0.4 mL in 100 mL POLYGLYCERYL-2 TRIISOSTEARATE (UNII: 68DUY2D39A) 2 mL in 100 mL LEMON OIL (UNII: I9GRO824LL) 0.1 mL in 100 mL DIPROPYLENE GLYCOL (UNII: E107L85C40) 0.2 mL in 100 mL LEVOMENTHOL (UNII: BZ1R15MTK7) 0.1 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75504-170-11 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/29/2020 Labeler - Kora Holdings LLC (695692001) Establishment Name Address ID/FEI Business Operations Sellus 690026575 manufacture(75504-170)