Home NDC 63083-2068-2 Female Formula
Product NDC 63083-2068
Requested package NDC 63083-2068-2
11-digit product format 630832068
Labeler code 63083
Product ID 63083-2068_f11fffdb-c427-40c3-ad87-ee5143d3ecb7
Type HUMAN OTC DRUG
Nonproprietary name Female Formula
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance CNIDIUM MONNIERI FRUIT; CYPERUS ROTUNDUS TUBER; GLYCYRRHIZA GLABRA; REHMANNIA GLUTINOSA ROOT; JUJUBE FRUIT; ANGELICA ACUTILOBA ROOT; CODONOPSIS PILOSULA ROOT; ATRACTYLODES MACROCEPHALA ROOT
Active strength 3; 3; 3; 3; 3; 3; 3; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 Female Formula
Brand name suffix 2068
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CNIDIUM MONNIERI FRUIT 3 [hp_X]/59mL CYPERUS ROTUNDUS TUBER 3 [hp_X]/59mL GLYCYRRHIZA GLABRA 3 [hp_X]/59mL REHMANNIA GLUTINOSA ROOT 3 [hp_X]/59mL JUJUBE FRUIT 3 [hp_X]/59mL ANGELICA ACUTILOBA ROOT 3 [hp_X]/59mL CODONOPSIS PILOSULA ROOT 3 [hp_X]/59mL ATRACTYLODES MACROCEPHALA ROOT 3 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
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 C68 2026-01-09 C68 2024-01-30 C68 2024-01-30 C68
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2068-2 Female Formula2068 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 63083-2068 FEMALE FORMULA 2068 (FEMALE FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_e8d3990e-137c-4ae0-a702-7e50552c4294.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 63083-2068-2 63083206802 59 mL in 1 BOTTLE, DROPPER (63083-2068-2) 59 ml 1985-08-15 0000-00-00 No No Current