United States · FDA National Drug Code directory
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A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 21749-704_48373fc9-5f94-fd6d-e063-6294a90a1055
- Product NDC
- 21749-704
- Form
- GEL
- Composition / generic term
- alcohol
- Labeler
- GOJO Industries, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20120315
- Source listing expiry
- 20271231
Source-listed ingredients
- ALCOHOL — 70 mL/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 29 mL in 1 BOTTLE (21749-704-01) · 21749-704-01
- 59 mL in 1 BOTTLE (21749-704-02) · 21749-704-02
- 118 mL in 1 BOTTLE (21749-704-04) · 21749-704-04
- 236 mL in 1 BOTTLE (21749-704-08) · 21749-704-08
- 295 mL in 1 PACKAGE (21749-704-10) · 21749-704-10
- 354 mL in 1 BOTTLE (21749-704-12) · 21749-704-12
- 372 mL in 1 PACKAGE (21749-704-13) · 21749-704-13
- 1500 mL in 1 PACKAGE (21749-704-15) · 21749-704-15
- 2000 mL in 1 PACKAGE (21749-704-20) · 21749-704-20
- 710 mL in 1 PACKAGE (21749-704-24) · 21749-704-24
- 1000 mL in 1 PACKAGE (21749-704-33) · 21749-704-33
- 591 mL in 1 PACKAGE (21749-704-59) · 21749-704-59
- 192 mL in 1 PACKAGE (21749-704-65) · 21749-704-65
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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