Label: ALCHEMY LIVING HAND SANITIZER- ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75556-500-01 - Packager: ZHEJIANG SHUNAN INDUSTRY&TRADE CO.,LTD
- 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 14, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
For external use only: hands.
Flammable. Keep away from fire or flame.
When using this product
■ Keep out of eyes, ears, or mouth.
■ In case of eye contact, flush eyes thoroughly with water.
■ Avoid contact with broken skin.
■ Do not inhale or ingest.
Stop use and ask a doctor if
■ Redness or irritation develop
■ Condition persists for more than 72 hours.
Keep out of reach of children.
■ Children should be supervised by an adult when using this product.
■ If swallowed, get medical help or contact a Poison Control Center right away.
- Directions
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- STORAGE AND HANDLING
- KEEP OUT OF REACH OF CHILDREN
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
ALCHEMY LIVING HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75556-500 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 350 mL in 500 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75556-500-01 500 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 - ZHEJIANG SHUNAN INDUSTRY&TRADE CO.,LTD (528198838) Registrant - ZHEJIANG SHUNAN INDUSTRY&TRADE CO.,LTD (528198838) Establishment Name Address ID/FEI Business Operations ZHEJIANG SHUNAN INDUSTRY & TRADE CO., LTD 528198838 manufacture(75556-500)
