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Nasal Dryness Relief Gel

NDC 10738-051, Allantoin, gel, from Genuine Virgin Aloe Corporation.

Product NDC
10738-051
Status
Listed
Labeler
Genuine Virgin Aloe Corporation
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
505G(a)(3)
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10738-051 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALLANTOIN.5 g/100g
Package NDCNDC-11Package
10738-051-10107380051101 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 10738-051 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10738-051 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10738-051. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.