NDC 71919-821 30c Homeopathic Remedy Kit

50 Remedy Kit Kit Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
Product Characteristics
What is NDC 71919-821?
30c Homeopathic Remedy Kit Uses
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 71919-821 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:

71919-821

Proprietary Name:

30c Homeopathic Remedy Kit

Non-Proprietary Name: [1]

50 Remedy Kit

NDC Directory Status:

Human Otc Drug

Product Type: [3]

ACTIVE PRODUCT INCLUDED in the NDC Directory

Dosage Form:

Kit - A packaged collection of related material.

Administration Route(s): [4]

Oral - Administration to or by way of the mouth.

Labeler Name: [5]

Washington Homeopathic Products

Labeler Code:

71919

Product Label ID:

11e5ee81-1391-0dd3-e063-6294a90a5d0b

Marketing Category: [8]

UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Start Marketing Date: [9]

02-21-2024

Listing Expiration Date: [11]

12-31-2025

Exclude Flag: [12]

Code Navigator:

Product Characteristics

Color(s):

WHITE (C48325 - WHITE)

Code Structure Chart

Product Details

What is NDC 71919-821?

The NDC code 71919-821 is assigned by the FDA to the product 30c Homeopathic Remedy Kit which is a human over the counter drug product labeled by Washington Homeopathic Products. The generic name of 30c Homeopathic Remedy Kit is 50 remedy kit. The product's dosage form is kit and is administered via oral form. The product is distributed in a single package with assigned NDC code 71919-821-18 50 vial, glass in 1 kit / 1 kit in 1 vial, glass (71919-821-01) * 750 pellet in 1 vial, glass (68428-095-01) * 750 pellet in 1 vial, glass (68428-109-01) * 750 pellet in 1 vial, glass (68428-106-01) * 750 pellet in 1 vial, glass (68428-092-01) * 750 pellet in 1 vial, glass (68428-124-01) * 750 pellet in 1 vial, glass (68428-114-01) * 750 pellet in 1 vial, glass (68428-155-01) * 750 pellet in 1 vial, glass (68428-105-01) * 750 pellet in 1 vial, glass (68428-119-01) * 750 pellet in 1 vial, glass (68428-107-01) * 750 pellet in 1 vial, glass (68428-142-01) * 750 pellet in 1 vial, glass (68428-084-01) * 750 pellet in 1 vial, glass (68428-118-01) * 750 pellet in 1 vial, glass (68428-133-01) * 750 pellet in 1 vial, glass (68428-080-01) * 750 pellet in 1 vial, glass (68428-127-01) * 750 pellet in 1 vial, glass (68428-156-01) * 750 pellet in 1 vial, glass (68428-147-01) * 750 pellet in 1 vial, glass (68428-138-01) * 750 pellet in 1 vial, glass (68428-103-01) * 750 pellet in 1 vial, glass (68428-148-01) * 750 pellet in 1 vial, glass (68428-122-01) * 750 pellet in 1 vial, glass (68428-154-01) * 750 pellet in 1 vial, glass (68428-112-01) * 750 pellet in 1 vial, glass (68428-099-01) * 750 pellet in 1 vial, glass (68428-146-01) * 750 pellet in 1 vial, glass (68428-091-01) * 750 pellet in 1 vial, glass (68428-115-01) * 750 pellet in 1 vial, glass (68428-111-01) * 750 pellet in 1 vial, glass (68428-098-01) * 750 pellet in 1 vial, glass (68428-144-01) * 750 pellet in 1 vial, glass (68428-102-01) * 750 pellet in 1 vial, glass (68428-090-01) * 750 pellet in 1 vial, glass (68428-083-01) * 750 pellet in 1 vial, glass (68428-082-01) * 750 pellet in 1 vial, glass (68428-078-01) * 750 pellet in 1 vial, glass (68428-108-01) * 350 pellet in 1 vial, glass (71919-768-01) * 750 pellet in 1 vial, glass (68428-097-01) * 750 pellet in 1 vial, glass (68428-086-01) * 750 pellet in 1 vial, glass (68428-134-01) * 750 pellet in 1 vial, glass (68428-149-01) * 750 pellet in 1 vial, glass (68428-131-01) * 750 pellet in 1 vial, glass (68428-104-01) * 750 pellet in 1 vial, glass (68428-085-01) * 750 pellet in 1 vial, glass (68428-125-01) * 750 pellet in 1 vial, glass (68428-123-01) * 750 pellet in 1 vial, glass (68428-101-01) * 750 pellet in 1 vial, glass (68428-117-01) * 750 pellet in 1 vial, glass (68428-077-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for 30c Homeopathic Remedy Kit?

Acon nap fearAesculus hipp hemorrhoidsAllium cepa head coldAntimon crud wartsApis mel stingsArnica bruisesArsenicum alb vomitingBelladonna feverBellis bruised sorenessBerber vulg itchingBryonia worse motionCalc carb overworkCaulophyllum crampsCausticum hoarsenessChamomilla irritabilityCimicifuga minor back painCoffea cruda sleeplessnessDrosera coughEupatorium perf flu-like symptomsEuphrasia eye irritationFerrum phos low feverGelsemium lethargyHamamelis varicose veinsHepar sulph calc croupinessHydrastis sinusesHypericum shooting painIgnatia sadnessIpecac nauseaKali bic sinusesKali carb sour belchingKali mur congested earsKali phos irritabilityLachesis sore throatLedum black eyesLycopodium digestionMag phos crampsNat mur sneezingNux vom vomitingPetroleum nauseaPhosphoricum ac headachePhytolacca sore throatPodoph pelt diarrheaPulsatilla weepingRhus tox better motionRuta bruised feelingSepia indifferenceStaphysag angerSulphur skin problemsSymphytum prickling painThuja occ warts

Which are 30c Homeopathic Remedy Kit UNII Codes?

The UNII codes for the active ingredients in this product are:

ACONITUM NAPELLUS (UNII: U0NQ8555JD)
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
ARABICA COFFEE BEAN (UNII: 3SW678MX72)
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
CALCIUM SULFIDE (UNII: 1MBW07J51Q)
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
SULFUR (UNII: 70FD1KFU70)
SULFUR (UNII: 70FD1KFU70) (Active Moiety)
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
BRYONIA ALBA ROOT (UNII: T7J046YI2B)
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
IPECAC (UNII: 62I3C8233L)
IPECAC (UNII: 62I3C8233L) (Active Moiety)
ANTIMONY TRISULFIDE (UNII: F79059A38U)
ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
EUPHRASIA STRICTA (UNII: C9642I91WL)
EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
GOLDENSEAL (UNII: ZW3Z11D0JV)
GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
ONION (UNII: 492225Q21H)
ONION (UNII: 492225Q21H) (Active Moiety)
ARNICA MONTANA (UNII: O80TY208ZW)
ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
ARSENIC TRIOXIDE (UNII: S7V92P67HO)
ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
PULSATILLA VULGARIS (UNII: I76KB35JEV)
PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
CAUSTICUM (UNII: DD5FO1WKFU)
CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
KEROSENE (UNII: 1C89KKC04E)
KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
BLACK COHOSH (UNII: K73E24S6X9)
BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
PODOPHYLLUM (UNII: 2S713A4VP3)
PODOPHYLLUM (UNII: 2S713A4VP3) (Active Moiety)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
APIS MELLIFERA (UNII: 7S82P3R43Z)
APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
BELLIS PERENNIS (UNII: 2HU33I03UY)
BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
DROSERA ROTUNDIFOLIA (UNII: 75O014T1HG)
DROSERA ROTUNDIFOLIA (UNII: 75O014T1HG) (Active Moiety)
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
POTASSIUM DICHROMATE (UNII: T4423S18FM)
DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
PHOSPHORIC ACID (UNII: E4GA8884NN)
PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
COMFREY ROOT (UNII: M9VVZ08EKQ)
COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
LACHESIS MUTA VENOM (UNII: VSW71SS07I)
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
TOXICODENDRON RADICANS LEAF (UNII: CDH3461U7L)
TOXICODENDRON RADICANS LEAF (UNII: CDH3461U7L) (Active Moiety)

Which are 30c Homeopathic Remedy Kit Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
SUCROSE (UNII: C151H8M554)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".

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