NDC 53405-0004 E.o.l.

Stillingia Sylvatica, Zincum Gluconicum, Thiaminum Hydrochloricum, Fragaria Vescus, Niacin, Serotonin (hydrochloride), 5-hydroxytryptophan, Betainum Muriaticum

NDC Product Code 53405-0004

NDC Code: 53405-0004

Proprietary Name: E.o.l. What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Stillingia Sylvatica, Zincum Gluconicum, Thiaminum Hydrochloricum, Fragaria Vescus, Niacin, Serotonin (hydrochloride), 5-hydroxytryptophan, Betainum Muriaticum 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.

NDC Code Structure

  • 53405 - Inlight Creation, Llc.
    • 53405-0004 - E.o.l.

NDC 53405-0004-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

E.o.l. with NDC 53405-0004 is a a human over the counter drug product labeled by Inlight Creation, Llc.. The generic name of E.o.l. is stillingia sylvatica, zincum gluconicum, thiaminum hydrochloricum, fragaria vescus, niacin, serotonin (hydrochloride), 5-hydroxytryptophan, betainum muriaticum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Inlight Creation, Llc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

E.o.l. Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
  • ZINC GLUCONATE 3 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 4 [hp_X]/mL
  • ALPINE STRAWBERRY 5 [hp_X]/mL
  • NIACIN 5 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 5 [hp_X]/mL
  • OXITRIPTAN 6 [hp_X]/mL
  • BETAINE HYDROCHLORIDE 6 [hp_X]/mL
  • BIOTIN 6 [hp_X]/mL
  • CHOLINE HYDROXIDE 6 [hp_X]/mL
  • UBIDECARENONE 6 [hp_X]/mL
  • CYSTEINE 6 [hp_X]/mL
  • RACEMETHIONINE 6 [hp_X]/mL
  • ALANINE 6 [hp_X]/mL
  • CYSTINE 6 [hp_X]/mL
  • GLUTAMIC ACID 6 [hp_X]/mL
  • GLUTAMINE 6 [hp_X]/mL
  • LYSINE 6 [hp_X]/mL
  • METHIONINE 6 [hp_X]/mL
  • SERINE 6 [hp_X]/mL
  • AMINOBENZOIC ACID 6 [hp_X]/mL
  • POTASSIUM GLUCONATE 6 [hp_X]/mL
  • SUS SCROFA THYMUS 6 [hp_X]/mL
  • THYROID, PORCINE 6 [hp_X]/mL
  • CHOLECALCIFEROL 6 [hp_X]/mL
  • CRANBERRY 7 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 7 [hp_X]/mL
  • LITHIUM BROMIDE 7 [hp_X]/mL
  • SHARK CARTILAGE 7 [hp_X]/mL
  • SQUALENE 7 [hp_X]/mL
  • COPPER 8 [hp_X]/mL
  • PHENYLALANINE 8 [hp_X]/mL
  • SELENIUM DIOXIDE 8 [hp_X]/mL
  • SELENIUM 8 [hp_X]/mL
  • BORRELIA BURGDORFERI 12 [hp_X]/mL
  • COCONUT OIL 12 [hp_X]/mL
  • CANDIDA ALBICANS 12 [hp_X]/mL
  • PUMPKIN SEED 17 [hp_X]/mL
  • LEMON JUICE 18 [hp_X]/mL
  • BROMELAINS 6 [hp_C]/mL
  • AESCULUS HIPPOCASTANUM FLOWER 30 [hp_C]/mL
  • ILEX AQUIFOLIUM FLOWERING TOP 30 [hp_C]/mL
  • MALUS DOMESTICA FLOWER 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Inlight Creation, Llc.
Labeler Code: 53405
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 07-07-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 12-24-2019 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

E.o.l. Product Label Images

E.o.l. Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Stillingia Sylvatica 3X, Zincum Gluconicum 3X, Thiaminum Hydrochloricum 4X, Fragaria Vesca 5X, Niacin 5X, Serotonin (Hydrochloride) 5X, 5-Hydroxtryptophan 6X, Betainum Muriaticum 6X, Biotin 6X, Cholinum 6X, Co-Enzyme Q-10 6X, Cysteinum 6X, Dl-Methionine 6X, L-Alanine 6X, L-Cystine 6X, L-Glutamine acid 6X, L-Glutamine 6X, L-Lysine 6X, L-Methionine 6X. L-Serine 6X, Paba 6X, Potassium Gluconate 6X, Thymus (suis) 6x, Throidinum (suis) 6X, Vitamin D3 6X, Cranberry 7X, Dopamine Hydrochloride 7X, Lithium Bromatum 7X, Shark Cartilage 7X, Squalene 7X, Cuprum Metallicum 8X, Phenylalanine 8X, Selenium Dioxide 8X, Selenium Metallicum 8X, Borrelia Burgdorferi Nosode 12X, Coconut oil 12X, Candida Albicans 12X,30X,12C,30C, Cucurbita Pepo,semen 17X, Citrus Limonum 18X, Bromelain 6C, Aesculus Hippocastanum, Flos 30C, Ilex Aquifolium, Flos 30C, Malus Pumila, Flos 30C

Indications:

Support of fingernails, hair and skin.

Support of fingernails, hair and skin.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in cool, dry place

Keep Out Of Reach Of Children.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by InLight Creation, LLC.3395 South Jones Blvd, Ste. #28Las Vegas, NV  89146775-400-119

Package Label Dispaly:

InLight CreationE.O.LHOMEOPATHIC REMEDY2 fl. oz. (60 ml)

* Please review the disclaimer below.

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