Pilocarpine Hydrochloride Solution/ Drops
Product Images NDC 70069-181

7 FDA label images from Somerset Therapeutics, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Pilocarpine Hydrochloride (NDC 70069-181). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image (51d33ccf C470 4240 Bdb5 34a609518615 01)

Image (51d33ccf C470 4240 Bdb5 34a609518615 01)
Chemical structure of Pilocarpine Hydrochloride, depicted as a molecular diagram showing the arrangement of carbon, hydrogen, nitrogen, oxygen atoms, and the hydrochloride group.*
FDA Label Image

Container 1% (51d33ccf C470 4240 Bdb5 34a609518615 02)

Container 1% (51d33ccf C470 4240 Bdb5 34a609518615 02)
Pilocarpine Hydrochloride 1% Ophthalmic Solution USP 15 mL bottle label showing active ingredient pilocarpine hydrochloride 1%, preservative benzalkonium chloride 0.01%, and several inactive ingredients. The product is sterile and for topical ophthalmic use only. It is manufactured for Somerset Therapeutics, LLC, made in India, and includes storage instructions and usual dosage guidelines. The label includes a barcode and NDC 70069-181-01.*
FDA Label Image

Carton 1% (51d33ccf C470 4240 Bdb5 34a609518615 03)

Carton 1% (51d33ccf C470 4240 Bdb5 34a609518615 03)
Label for Pilocarpine HCl Ophthalmic Solution, USP 1% in 15 mL bottles by Somerset Therapeutics, LLC. The label states Rx only and includes ingredients listing pilocarpine hydrochloride 1% as active and benzalkonium chloride 0.01% as preservative. It specifies ophthalmic use only, sterile solution, and storage instructions. Barcodes and manufacturer contact information are present.*
FDA Label Image

Container 2% (51d33ccf C470 4240 Bdb5 34a609518615 04)

Container 2% (51d33ccf C470 4240 Bdb5 34a609518615 04)
Label for Pilocarpine HCl Ophthalmic Solution USP 2%, an ophthalmic solution for topical use supplied in a 15 mL volume. The label includes the active ingredient concentration, preservative and inactive ingredients, storage instructions, a barcode, and indicates the product is sterile and for Rx only. Manufactured for Somerset Therapeutics, LLC.*
FDA Label Image

Carton 2% (51d33ccf C470 4240 Bdb5 34a609518615 05)

Carton 2% (51d33ccf C470 4240 Bdb5 34a609518615 05)
Label for Pilocarpine HCl Ophthalmic Solution, USP 2%, 15 mL by Somerset Therapeutics LLC. The product is Rx only for topical ophthalmic use. Active ingredient is pilocarpine hydrochloride 2%, with preservatives and inactives listed. Storage instructions and usual dosage directions are included. The label features barcodes, manufacturer info, and the Somerset Therapeutics logo.*
FDA Label Image

Container 4% (51d33ccf C470 4240 Bdb5 34a609518615 06)

Container 4% (51d33ccf C470 4240 Bdb5 34a609518615 06)
Label for Pilocarpine HCl Ophthalmic Solution, USP 4%, a sterile solution for topical ophthalmic use. The label notes 15 mL volume, active ingredient pilocarpine hydrochloride 4%, and preservatives including benzalkonium chloride 0.01%. Manufactured for Somerset Therapeutics, LLC, with storage instructions and usual dosage information also shown.*
FDA Label Image

Carton 4% (51d33ccf C470 4240 Bdb5 34a609518615 07)

Carton 4% (51d33ccf C470 4240 Bdb5 34a609518615 07)
Packaging label for Pilocarpine HCl Ophthalmic Solution, USP 4% in a 15 mL bottle. The label identifies the product as sterile and for topical ophthalmic use only. Manufactured for Somerset Therapeutics, LLC, the label includes ingredient details, barcode, NDC 70069-201-01, and storage instructions. The Somerset Therapeutics logo is displayed at the bottom.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.