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GenRx Anti-Bacterial Gel

NDC 59088-299, Alcohol, liquid, from PureTek Corporation.

Product NDC
59088-299
Status
Listed
Labeler
PureTek Corporation
Dosage form
LIQUID
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M014
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALCOHOL62 mL/100mL
Package NDCNDC-11Package
59088-299-0859088029908118 mL in 1 BOTTLE, PUMP (59088-299-08)
59088-299-3159088029931500 mL in 1 BOTTLE, DISPENSING (59088-299-31)
59088-299-3959088029939710 mL in 1 BOTTLE, PUMP (59088-299-39)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

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

Use it

Look up 59088-299 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-299. 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.