Label: HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E- alcohol liquid
- NDC Code(s): 55319-505-34
- Packager: Family Dollar Services Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- ACTIVE INGREDIENT
Ethyl Alcohol 65%Close
- INDICATIONS & USAGE
Uses• hand sanitizer to help reduce bacteria on the skin. • recommended for repeated useClose
Warnings • Flammable • Keep away from fire or flame • For external use onlyClose
- WHEN USING
When using this product • avoid contact with eyes • in case of eye contact immediately flush eyes with water, call a doctor • avoid contact with broken skin
Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.Close
- KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children. Children should only use this product under adult supervision.
Do not drink. Not edible. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away.Close
- SPL UNCLASSIFIED SECTION
Other Information •do not store above 105F. May discolor some fabrics • Harmful to wood finishes and plasticsClose
- DOSAGE & ADMINISTRATION
Directions •place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry • recommended for repeated use.Close
- INACTIVE INGREDIENT
Inactive ingredients aloe barbadensis leaf extract, caprylyl glycol, carbomer, dimethicone, fragrance, phenoxyethanol, propylene glycol, tocopheryl acetate, triethanolamine, water.Close
- INGREDIENTS AND APPEARANCE
HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-505 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 65 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55319-505-34 10 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/01/2012 Labeler - Family Dollar Services Inc. (024472631)