Label: PURELL ADVANCED HAND SANITIZER ASPEN RETREAT - alcohol gel
- NDC Code(s): 21749-252-01
- Packager: GOJO Industries, 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 70% v/vClose
Hand sanitizer to help reduce bacteria on the skinClose
Flammable. Keep away from fire or flame.
For external use only.
- WHEN USING
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.Close
- STOP USE
Stop use and ask a doctor if irritation or rash appears and lasts.Close
- KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.Close
Place enough product in your palm to thoroughly cover you hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this productClose
- Inactive ingredients
Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Glycerin, Isopropyl Myristate, Lactose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Cellulose, Hydroxypropyl Methylcellulose, Fragrance (Parfum), Blue 1 (CI 42090), Red 33 (CI 17200), Ultramarines (CI 77007), Yellow 5 (CI 19140)Close
- Package Label
PURELL® Advanced Hand Sanitizer Aspen Retreat
Kills the Most Germs* *Ounce for ounce outperforms PURELL® original formulations when used on hands as directed
Kills more than 99.99% of most common germs that may make you sick.
GOJO Industries, Inc.
Akron, OH 44309
Questions? Tel: 1-888-4-PURELL www.PURELL.com
(c)2012. GOJO Industries, Inc.
- INGREDIENTS AND APPEARANCE
PURELL ADVANCED HAND SANITIZER ASPEN RETREAT
Product Information Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:21749-252 Route of Administration TOPICAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (ALCOHOL) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength Water ISOPROPYL ALCOHOL CAPRYLYL GLYCOL GLYCERIN ISOPROPYL MYRISTATE LACTOSE .ALPHA.-TOCOPHEROL ACETATE CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) AMINOMETHYLPROPANOL POWDERED CELLULOSE HYPROMELLOSES FD&C BLUE NO. 1 D&C RED NO. 33 ULTRAMARINE BLUE FD&C YELLOW NO. 5 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-252-01 30 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/01/2012 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-252)