Home NDC 81056-8001 80% Alcohol Hand Sanitizer
Product NDC 81056-8001
11-digit product format 810568001
Labeler code 81056
Product ID 81056-8001_b362cd95-5ab2-bd53-e053-2995a90a7482
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL SANITIZER
Dosage form LIQUID
Route AURICULAR (OTIC); BUCCAL; CONJUNCTIVAL; DENTAL; ELECTRO-OSMOSIS; ENDOCERVICAL; ENDOSINUSIAL; ENDOTRACHEAL; ENTERAL; EPIDURAL; EXTRA-AMNIOTIC; EXTRACORPOREAL; HEMODIALYSIS; INFILTRATION; INTERSTITIAL; INTRA-ABDOMINAL; INTRA-AMNIOTIC; INTRA-ARTERIAL; INTRA-ARTICULAR; INTRABILIARY; INTRABRONCHIAL; INTRABURSAL; INTRACAMERAL; INTRACANALICULAR; INTRACARDIAC; INTRACARTILAGINOUS; INTRACAUDAL; INTRACAVERNOUS; INTRACAVITARY; INTRACEREBRAL; INTRACISTERNAL; INTRACORNEAL; INTRACORONAL, DENTAL; INTRACORONARY; INTRACORPORUS CAVERNOSUM; INTRACRANIAL; INTRADERMAL; INTRADISCAL; INTRADUCTAL; INTRADUODENAL; INTRADURAL; INTRAEPICARDIAL; INTRAEPIDERMAL; INTRAESOPHAGEAL; INTRAGASTRIC; INTRAGINGIVAL; INTRAHEPATIC; INTRAILEAL; INTRALESIONAL; INTRALINGUAL; INTRALUMINAL; INTRALYMPHATIC; INTRAMAMMARY; INTRAMEDULLARY; INTRAMENINGEAL; INTRAMUSCULAR; INTRANODAL; INTRAOCULAR; INTRAOMENTUM; INTRAOVARIAN; INTRAPERICARDIAL; INTRAPERITONEAL; INTRAPLEURAL; INTRAPROSTATIC; INTRAPULMONARY; INTRARUMINAL; INTRASINAL; INTRASPINAL; INTRASYNOVIAL; INTRATENDINOUS; INTRATESTICULAR; INTRATHECAL; INTRATHORACIC; INTRATUBULAR; INTRATUMOR; INTRATYMPANIC; INTRAUTERINE; INTRAVASCULAR; INTRAVENOUS; INTRAVENTRICULAR; INTRAVESICAL; INTRAVITREAL; IONTOPHORESIS; IRRIGATION; LARYNGEAL; NASAL; NASOGASTRIC; OCCLUSIVE DRESSING TECHNIQUE; OPHTHALMIC; ORAL; OROPHARYNGEAL; PARENTERAL; PERCUTANEOUS; PERIARTICULAR; PERIDURAL; PERINEURAL; PERIODONTAL; RECTAL; RESPIRATORY (INHALATION); RETROBULBAR; SOFT TISSUE; SUBARACHNOID; SUBCONJUNCTIVAL; SUBCUTANEOUS; SUBGINGIVAL; SUBLINGUAL; SUBMUCOSAL; SUBRETINAL; TRANSDERMAL; TRANSENDOCARDIAL; TRANSMUCOSAL; TRANSPLACENTAL; TRANSTRACHEAL; TRANSTYMPANIC; URETERAL; URETHRAL; VAGINAL
Labeler THE PAINT COMPANY OF NC INC
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-12-01
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 80 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 40 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 81056-8001-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 81056-8001-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 81056-8001-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 81056-8001-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 81056-8001-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 81056-8001-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 81056-8001-1 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 81056-8001-1 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81056-8001-1 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 81056-8001-1 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 81056-8001-1 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 81056-8001-1 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 81056-8001-1 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 81056-8001-1 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 81056-8001-1 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 81056-8001-1 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 81056-8001-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 81056-8001-1 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product E Excluded after deficient or non-compliant submission was not corrected 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 81056-8001-1 E Excluded after deficient or non-compliant submission was not corrected 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product Y Unknown FDA exclusion code: Y e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 81056-8001-1 Y Unknown FDA exclusion code: Y e2bbac7714bc…27bdfed8d636…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81056-8001-1 80% Alcohol Hand Sanitizer 1 mL in 1 BOTTLE LIQUID 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81056-8001 80% ALCOHOL HAND SANITIZER (ALCOHOL SANITIZER) LIQUID [THE PAINT COMPANY OF NC INC] 1 Legacy NDC, 1 package rows 20201201_b362b3bd-dda4-f0af-e053-2a95a90aaa49.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 81056-8001-1 81056800101 1 mL in 1 BOTTLE 1 ml Historical