dr. talbots

Generic: ethyl alcohol

Labeler: talbots pharmaceuticals family products, llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dr. talbots
Generic Name ethyl alcohol
Labeler talbots pharmaceuticals family products, llc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol 75 mL/100mL

Manufacturer
Talbots Pharmaceuticals Family Products, LLC.

Identifiers & Regulatory

Product NDC 70797-160
Product ID 70797-160_2b380620-3e8e-77b0-e063-6394a90a9442
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M014
Listing Expiration 2026-12-31
Marketing Start 2020-05-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70797160
Hyphenated Format 70797-160

Supplemental Identifiers

RxCUI
1305100
UNII
3K9958V90M

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dr. talbots (source: ndc)
Generic Name ethyl alcohol (source: ndc)
Application Number M014 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 75 mL/100mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE (70797-160-01)
  • 250 mL in 1 BOTTLE, PUMP (70797-160-02)
  • 500 mL in 1 BOTTLE, PUMP (70797-160-03)
  • 1000 mL in 1 BOTTLE, PUMP (70797-160-04)
source: ndc

Packages (4)

70797-160-01 50 mL in 1 BOTTLE (70797-160-01) 70797-160-02 250 mL in 1 BOTTLE, PUMP (70797-160-02) 70797-160-03 500 mL in 1 BOTTLE, PUMP (70797-160-03) 70797-160-04 1000 mL in 1 BOTTLE, PUMP (70797-160-04)

Ingredients (1)

alcohol (75 mL/100mL)

Linked Drug Pages (1)

Dr. Talbots ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2b380620-3e8e-77b0-e063-6394a90a9442", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1305100"], "spl_set_id": ["a6a94205-a9ff-7709-e053-2995a90a066b"], "manufacturer_name": ["Talbots Pharmaceuticals Family Products, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (70797-160-01)", "package_ndc": "70797-160-01", "marketing_start_date": "20200529"}, {"sample": false, "description": "250 mL in 1 BOTTLE, PUMP (70797-160-02)", "package_ndc": "70797-160-02", "marketing_start_date": "20200529"}, {"sample": false, "description": "500 mL in 1 BOTTLE, PUMP (70797-160-03)", "package_ndc": "70797-160-03", "marketing_start_date": "20200529"}, {"sample": false, "description": "1000 mL in 1 BOTTLE, PUMP (70797-160-04)", "package_ndc": "70797-160-04", "marketing_start_date": "20200529"}], "brand_name": "Dr. Talbots", "product_id": "70797-160_2b380620-3e8e-77b0-e063-6394a90a9442", "dosage_form": "GEL", "product_ndc": "70797-160", "generic_name": "Ethyl Alcohol", "labeler_name": "Talbots Pharmaceuticals Family Products, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr. Talbots", "active_ingredients": [{"name": "ALCOHOL", "strength": "75 mL/100mL"}], "application_number": "M014", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200529", "listing_expiration_date": "20261231"}