Label: PRO ADVANTAGE INSTANT HAND SANITIZER- alcohol gel
- NDC Code(s): 43128-118-04, 43128-118-05
- Packager: NDC National Distribution & Contracting, 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 March 15, 2023
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- Pro Advantage Instant Hand Sanitizer Gel
- Active Ingredients:
- Purpose
- Use
- Warning:
- When using this product
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions:
- Inactive Ingredients:
- REF: P779118 NDC 43128-118-04
- Product Labels
-
INGREDIENTS AND APPEARANCE
PRO ADVANTAGE INSTANT HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-118 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 620 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) DMDM HYDANTOIN (UNII: BYR0546TOW) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43128-118-04 1 in 1 PACKAGE 03/08/2013 1 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:43128-118-05 296 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/08/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/08/2013 Labeler - NDC National Distribution & Contracting, Inc. (009831413) Establishment Name Address ID/FEI Business Operations Dukal 088520668 manufacture(43128-118)