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Dr. Talbots

NDC 70797-160, Ethyl Alcohol, gel, from Talbot�s Pharmaceuticals Family Products, LLC..

Product NDC
70797-160
Status
Listed
Labeler
Talbot�s Pharmaceuticals Family Products, LLC.
Dosage form
GEL
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/70797-160 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALCOHOL75 mL/100mL
Package NDCNDC-11Package
70797-160-017079701600150 mL in 1 BOTTLE (70797-160-01)
70797-160-0270797016002250 mL in 1 BOTTLE, PUMP (70797-160-02)
70797-160-0370797016003500 mL in 1 BOTTLE, PUMP (70797-160-03)
70797-160-04707970160041000 mL in 1 BOTTLE, PUMP (70797-160-04)

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 70797-160 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70797-160 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70797-160. 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.