United States · FDA National Drug Code directory
Nasal Dryness Relief Gel
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
- 10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa
- Product NDC
- 10738-051
- Form
- GEL
- Composition / generic term
- Allantoin
- Labeler
- Genuine Virgin Aloe Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20220520
- Source listing expiry
- 20271231
Source-listed ingredients
- ALLANTOIN — .5 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15) · 10738-051-10
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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