United States · FDA National Drug Code directory
Purell Advanced Soothing
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
- 21749-713_5643056c-a2b5-b48a-e063-6394a90a6a5d
- Product NDC
- 21749-713
- Form
- GEL
- Composition / generic term
- alcohol
- Labeler
- GOJO Industries, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20181101
- Source listing expiry
- 20271231
Source-listed ingredients
- ALCOHOL — .7 mL/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE (21749-713-02) · 21749-713-02
- 118 mL in 1 PACKAGE (21749-713-04) · 21749-713-04
- 236 mL in 1 BOTTLE (21749-713-08) · 21749-713-08
- 295 mL in 1 PACKAGE (21749-713-10) · 21749-713-10
- 354 mL in 1 BOTTLE (21749-713-12) · 21749-713-12
- 710 mL in 1 PACKAGE (21749-713-24) · 21749-713-24
- 1000 mL in 1 PACKAGE (21749-713-33) · 21749-713-33
- 192 mL in 1 PACKAGE (21749-713-65) · 21749-713-65
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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