United States · FDA National Drug Code directory
Dr. Talbots
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
- 70797-160_2b380620-3e8e-77b0-e063-6394a90a9442
- Product NDC
- 70797-160
- Form
- GEL
- Composition / generic term
- Ethyl Alcohol
- Labeler
- Talbots Pharmaceuticals Family Products, LLC.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200529
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCOHOL — 75 mL/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BOTTLE (70797-160-01) · 70797-160-01
- 250 mL in 1 BOTTLE, PUMP (70797-160-02) · 70797-160-02
- 500 mL in 1 BOTTLE, PUMP (70797-160-03) · 70797-160-03
- 1000 mL in 1 BOTTLE, PUMP (70797-160-04) · 70797-160-04
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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