Label: XTRACARE INSTANT HAND SANITIZER - alcohol spray
- NDC Code(s): 57337-001-00, 57337-001-02
- Packager: Rejoice International
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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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- XtraCare instant Hand Sanitizer Spray
- Active ingredient
Ethyl Alcohol 62%Close
- hand sanitizer to help reduce bacteria on the skin that may cause disease.
- recommended for repeated use
Flammable. Keep away from fire or flame.
For external use only
When using this product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin.
Keep out of reach of children.
if swallowed, get medical help or contact a Poison Control Center right away.
- spray enough product in your palm to thoroughly cover your hands
- rub hands together briskly until dry
- children under 6 years of age should be supervised when using this product
- not recommended for infants
- Other Information
- store below 1050F (400C)
- may discolor certain fabrics or surfaces
- harmful to wood finishes and plastics
- store below 1050F (400C)
- Inactive ingredients
Water, Glycerin, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, FDandC Blue No. 1, FDandC Yellow No. 5.Close
instant Hand Sanitizer Spray Kills 99.9% of Germs Instantly
- Use anywhere without the need for water
- 100+sprays per bottle
DISTRIBUTED BY: REJOICE INTERNATIONAL INC. 48325 BINGHAMPTON DR, NOTRHVILLE, MI 48168, USAClose
MADE IN CHINA.
- PRINCIPAL DISPLAY PANEL
XtraCare instant Hand Sanitizer Spray 2 PK 100+SPRAYS Kills 99.9% of Germs Instantly Leaves hands feeling soft with Aloe and Vitamin E Convenient Size for Purse, Pocket or Car PERFECT FOR TRAVEL 2x0.34 fl oz(2x10 ml)Close
- Product Labels
- INGREDIENTS AND APPEARANCE
XTRACARE INSTANT HAND SANITIZER
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57337-001 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57337-001-02 2 in 1 PACKAGE 1 NDC:57337-001-00 10 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333E 02/08/2013 Labeler - Rejoice International (078741245) Establishment Name Address ID/FEI Business Operations Ningbo Unichem 528196956 manufacture(57337-001)