Travel Sickness Drops

Product NDC
63083-2075
11-digit product format
630832075
Labeler code
63083
Product ID
63083-2075_b63aaff8-bc82-4834-bb1e-c9b2e62e5bf5
Type
HUMAN OTC DRUG
Nonproprietary name
Travel Sickness Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
AETHUSA CYNAPIUM WHOLE; AMBERGRIS; ANAMIRTA COCCULUS FRUIT; APOMORPHINE HYDROCHLORIDE; COLCHICUM AUTUMNALE BULB; IPECAC; LIQUID PETROLEUM; STRYCHNOS NUX-VOMICA SEED; VERATRUM ALBUM ROOT
Active strength
6; 12; 12; 12; 12; 6; 12; 30; 30 [hp_X]/59mL; [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], Dopamine Agonists [MoA], Dopaminergic Agonist [EPC], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Travel Sickness Drops
Brand name suffix
2075
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AETHUSA CYNAPIUM WHOLE6 [hp_X]/59mL
AMBERGRIS12 [hp_X]/59mL
ANAMIRTA COCCULUS FRUIT12 [hp_X]/59mL
APOMORPHINE HYDROCHLORIDE12 [hp_X]/59mL
COLCHICUM AUTUMNALE BULB12 [hp_X]/59mL
IPECAC6 [hp_X]/59mL
LIQUID PETROLEUM12 [hp_X]/59mL
STRYCHNOS NUX-VOMICA SEED30 [hp_X]/59mL
VERATRUM ALBUM ROOT30 [hp_X]/59mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiM6936L953C, XTC0D02P6C, 3E8XBL6YYK, F39049Y068, 993QHL78E6, 62I3C8233L, 6ZAE7X688J, 269XH13919, QNS6W5US1Z

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8cacec2b-1363-4e94-885c-4189d5e7208aProduct name120251117
d7fea1a2-3459-27e8-1231-1b79988f4937Product name220221207
3a53909e-cbfb-4956-984e-a33101906fd9Product name120201021

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2075-22026-01-09C16284748780-11030e365-6818-111a-e063-dadaa90a10e2C75
63083-2075-22026-01-09C16284748780-11030e365-6818-111a-e063-dadaa90a10e2C75
63083-2075-22024-01-30C16284748780-11030e365-6818-111a-e063-dadaa90a10e2C75
63083-2075-22024-01-30C16284748780-11030e365-6818-111a-e063-dadaa90a10e2C75

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2075-2Travel Sickness Drops207559 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2075TRAVEL SICKNESS DROPS 2075 (TRAVEL SICKNESS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220216_8c9d93bc-a055-458a-8cc0-c984b4b754c0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2075-26308320750259 mL in 1 BOTTLE, DROPPER (63083-2075-2) 59 ml1985-08-150000-00-00NoNoCurrent