Label: HAND SANITIZER CITRUS BLEND- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 70338-606-22 - Packager: MedZone Products, 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 June 17, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purposes
- Uses:
- Warnings:
- Do not use:
- KEEP OUT OF REACH OF CHILDREN
- When using this product:
- Stop use and ask a doctor
- Directions:
- Inactive Ingredients:
- Other:
- SPL UNCLASSIFIED SECTION
- Questions?
- PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HAND SANITIZER CITRUS BLEND
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70338-606 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 HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) ORANGE OIL (UNII: AKN3KSD11B) LEMON OIL (UNII: I9GRO824LL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70338-606-22 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/17/2020 Labeler - MedZone Products, LLC (080083739) Establishment Name Address ID/FEI Business Operations Our Babylon LLC 105266218 manufacture(70338-606)