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  3. Human OTC Drug
  4. Pink Eye

Pink Eye

Belladonna, Euphrasia Officinalis, Hepar Sulphuris


Cvs Pharmacy
Human Otc Drug
NDC 69842-901
Pink Eye also known as Belladonna, Euphrasia Officinalis, Hepar Sulphuris is a human otc drug labeled by 'Cvs Pharmacy'. National Drug Code (NDC) number for Pink Eye is 69842-901. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Pink Eye drug includes Atropa Belladonna - 6 [hp_X]/10mL Calcium Sulfide - 12 [hp_X]/10mL Euphrasia Stricta - 6 [hp_X]/10mL . The currest status of Pink Eye drug is Active.

Drug Information:

Drug NDC: 69842-901
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Pink Eye
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Belladonna, Euphrasia Officinalis, Hepar Sulphuris
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Cvs Pharmacy
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Solution/ Drops
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ATROPA BELLADONNA - 6 [hp_X]/10mL
CALCIUM SULFIDE - 12 [hp_X]/10mL
EUPHRASIA STRICTA - 6 [hp_X]/10mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:OPHTHALMIC
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 15 Feb, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 18 Dec, 2025
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.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:CVS Pharmacy
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:WQZ3G9PF0H
1MBW07J51Q
C9642I91WL
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
69842-901-111 BOTTLE, DROPPER in 1 CARTON (69842-901-11) / 10 mL in 1 BOTTLE, DROPPER15 Feb, 2019N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.
Other medicines with the same generic name

Pink Eye


Belladonna, Euphrasia Officinalis, Hepar Sulphuris

Solution/ Drops
CVS Pharmacy
NDC: 69842-901

Pink Eye Nighttime


Belladonna, Euphrasia Officinalis, Hepar Sulphuris

Gel
Similasan AG
NDC: 53799-377

Pink Eye Relief


Belladonna, Euphrasia Officinalis, Hepar Sulphuris

Solution/ Drops
Similasan AG
NDC: 53799-365

Pink Eye Relief


Belladonna, Euphrasia Officinalis, Hepar Sulphuris

Solution/ Drops
Similasan Corporation
NDC: 59262-365

Pink Eye Nighttime


Belladonna, Euphrasia Officinalis, Hepar Sulphuris

Gel
Similasan Corporation
NDC: 59262-377

Purpose:

Purpose dryness, redness, burning, sensation of grittiness watery discharge redness, stinging

Product Elements:

Pink eye belladonna, euphrasia officinalis, hepar sulphuris atropa belladonna atropa belladonna euphrasia stricta euphrasia stricta calcium sulfide calcium sulfide water silver sulfate sodium nitrate

Indications and Usage:

Uses** according to homeopathic principles, the active ingredients in this product temporarily relieve minor eye symptoms: • excessive watery (clear) discharge • sensation of grittiness • redness and burning

Warnings:

Warnings • for external use only. • children under 2 years of age should be seen by a physician. • according to homeopathic principles, symptoms may temporarily worsen before improving (initial exacerbation of symptoms). • to avoid contamination, do not touch the tip of the bottle to any surface. • to avoid contamination use within 30 days of opening. expiration date only refers to unopened bottle. • replace cap tightly after every use. • contact wearers: consult physician prior to using. if pregnant, trying to get pregnant or breast feeding, ask a health professional before use. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away. do not use: • if the solution changes color or becomes cloudy stop use and ask a doctor if: • you experience eye pain or changes in vision • symptoms worsen or persist for more than 72 hours • you might have a serious underlying medical cause for an
infection

Do Not Use:

Warnings • for external use only. • children under 2 years of age should be seen by a physician. • according to homeopathic principles, symptoms may temporarily worsen before improving (initial exacerbation of symptoms). • to avoid contamination, do not touch the tip of the bottle to any surface. • to avoid contamination use within 30 days of opening. expiration date only refers to unopened bottle. • replace cap tightly after every use. • contact wearers: consult physician prior to using. if pregnant, trying to get pregnant or breast feeding, ask a health professional before use. keep out of reach of children. if swallowed, get medical help or contact a poison control center right away. do not use: • if the solution changes color or becomes cloudy stop use and ask a doctor if: • you experience eye pain or changes in vision • symptoms worsen or persist for more than 72 hours • you might have a serious underlying medical cause for an infection

Dosage and Administration:

Directions for adults and children ages 2 and over: • remove tamper-evident seal from neck of bottle • twist cap off bottle • don’t squeeze bottle, squeeze plastic tip to release 2-3 drops into eye • apply as needed • replace cap after use

Stop Use:

Stop use and ask a doctor if: • you experience eye pain or changes in vision • symptoms worsen or persist for more than 72 hours • you might have a serious underlying medical cause for an infection

Package Label Principal Display Panel:

Principal display panel pink eye drops sterile eye drops 10 ml (0.33 fl oz) principal display panel pink eye drops sterile eye drops 10 ml (0.33 fl oz)


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.

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