Label: EVELINE CHARLES HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 76555-001-01, 76555-001-02, 76555-001-03, 76555-001-04, view more76555-001-05, 76555-001-06, 76555-001-07 - Packager: Ec Labs Inc
- 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 June 5, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use
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Warnings
For external use only
Flammability warning. Keep away from open flame and sources of heat
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if irritation develops.
Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away. - Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EVELINE CHARLES HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76555-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 72 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 2 g in 100 g ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.05 g in 100 g WATER (UNII: 059QF0KO0R) 25.15 g in 100 g CARBOMER 940 (UNII: 4Q93RCW27E) 0.55 g in 100 g TROLAMINE (UNII: 9O3K93S3TK) 0.25 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76555-001-01 60 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 2 NDC:76555-001-02 240 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 3 NDC:76555-001-03 296 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 4 NDC:76555-001-04 500 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 5 NDC:76555-001-05 750 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 6 NDC:76555-001-06 1000 g in 1 BOTTLE; Type 0: Not a Combination Product 06/05/2020 7 NDC:76555-001-07 4000 g in 1 JUG; Type 0: Not a Combination Product 06/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/05/2020 Labeler - Ec Labs Inc (205510751) Registrant - Ec Labs Inc (205510751) Establishment Name Address ID/FEI Business Operations Ec Labs Inc 205510751 manufacture(76555-001) , pack(76555-001) , label(76555-001)