Home NDC 63083-4019-2 Human Papillomavirus Combination
Product NDC 63083-4019
Requested package NDC 63083-4019-2
11-digit product format 630834019
Labeler code 63083
Product ID 63083-4019_715066f7-85c1-4f41-9b6c-96cfa5899aed
Type HUMAN OTC DRUG
Nonproprietary name Human Papillomavirus Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance HUMAN ADENOVIRUS B SEROTYPE 3; MUSA ACUMINATA WHOLE; HUMAN PAPILLOMAVIRUS SEROTYPE 16 WHOLE
Active strength 12; 12; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Human Papillomavirus Combination
Brand name suffix 4019
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HUMAN ADENOVIRUS B SEROTYPE 3 12 [hp_X]/59mL MUSA ACUMINATA WHOLE 12 [hp_X]/59mL HUMAN PAPILLOMAVIRUS SEROTYPE 16 WHOLE 30 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 740KW2J7GZ Internal UNII lookup 8O2MBI99WR Internal UNII lookup 063VBA799E Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 N19 2026-01-09 N19 2024-01-30 N19 2024-01-30 N19
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-4019-2 Human Papillomavirus Combination4019 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-4019 HUMAN PAPILLOMAVIRUS COMBINATION 4019 (HUMAN PAPILLOMAVIRUS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220301_de399089-a0b3-4d43-b1e9-fc361a91095b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-4019-2 63083401902 59 mL in 1 BOTTLE, DROPPER (63083-4019-2) 59 ml 1985-08-15 0000-00-00 No No Current