Label: EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E- ethyl alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 49035-557-03, 49035-557-12, 49035-557-34 - Packager: Wal-Mart Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 April 7, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
WARNINGS
For external use only: hands
Flammable, keep away from fire or flame.
When using this product
• keep out of eyes. In case of contact with eyes flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingestStop use and ask doctor if
- irritation and redness develop
- condition persists for more than 72 hours
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredient
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-557 Route of Administration TOPICAL 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) TROLAMINE (UNII: 9O3K93S3TK) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTHENOL (UNII: WV9CM0O67Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-557-03 89 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/07/2020 2 NDC:49035-557-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/07/2020 3 NDC:49035-557-34 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/07/2020 Labeler - Wal-Mart Stores, Inc. (051957769) Registrant - Wal-Mart Stores, Inc. (051957769)