Bicillin L-a Injection, Suspension
Product Images NDC 60793-702

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Bicillin L-a (NDC 60793-702). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer Inc, 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

Chem Structure (Bicillin 01)

Chem Structure (Bicillin 01)
Chemical structure of penicillin G benzathine, showing the core penicillin nucleus and benzathine moiety with associated water of hydration (4H2O). The structure highlights the beta-lactam ring, thiazolidine ring, and phenyl groups characteristic of penicillin.*
FDA Label Image

Logo (Bicillin 02)

Logo (Bicillin 02)
Pfizer Injectables product label showing distribution information. The label indicates the product is distributed by Pfizer Inc, located in New York, NY 10017. The Pfizer logo appears prominently at the top of the label.*
FDA Label Image

Principal Display Panel (1 mL Syringe Label)

Principal Display Panel (1 mL Syringe Label)
Label for BICILLIN L-A (penicillin G benzathine injectable suspension) showing a strength of 600,000 units per 1 mL. The label indicates it is for deep intramuscular injection, includes a warning about fatality if given by other routes, and lists Pfizer Inc as the distributor. The NDC number 60793-700-01 is also visible.*
FDA Label Image

Principal Display Panel (1 mL Syringe Carton)

Principal Display Panel (1 mL Syringe Carton)
Packaging label for Bicillin L-A injection, suspension, containing penicillin G benzathine at a strength of 600,000 units per 1 mL. The label indicates it is for pediatric use and deep intramuscular injection only. Manufactured by Pfizer Laboratories Div Pfizer Inc, the carton holds ten 1 mL syringes. Additional details include a warning about fatality if given by other routes and needle specifications (21 gauge, thin-wall, 1 inch needle).*
FDA Label Image

Principal Display Panel (2 mL Syringe Label)

Principal Display Panel (2 mL Syringe Label)
Label for BICILLIN L-A penicillin G benzathine injectable suspension 1,200,000 units per 2 mL, for deep intramuscular injection only. The label includes a warning in red that it is fatal if given by other routes. Distributed by Pfizer Inc, New York, NY. The NDC is 60793-701-02.*
FDA Label Image

Principal Display Panel (2 mL Syringe Carton)

Principal Display Panel (2 mL Syringe Carton)
Packaging label for BICILLIN L-A 1,200,000 units per 2 mL penicillin G benzathine injectable suspension. The carton states it contains ten 2 mL syringes for deep intramuscular injection only, distributed by Pfizer Inc. The label includes warnings, storage instructions, and specifies a 21 gauge, thin-wall, 1 ½ inch needle included with each syringe.*
FDA Label Image

Principal Display Panel (4 mL Syringe Label)

Principal Display Panel (4 mL Syringe Label)
BICILLIN L-A 2,400,000 units per 4 mL injectable suspension label for intramuscular use. The label displays the product name, active ingredient penicillin G benzathine, and the warning that it is fatal if given by other routes. Distributed by Pfizer Inc, New York, NY.*
FDA Label Image

Principal Display Panel (4 mL Syringe Carton)

Principal Display Panel (4 mL Syringe Carton)
Packaging label for BICILLIN L-A penicillin G benzathine injectable suspension, 2,400,000 units per 4 mL disposable syringe. The label indicates the product is for deep intramuscular injection only, distributed by Pfizer Inc. The label also notes the syringe size as 4 mL and includes warnings about administration routes and instructions. The package has Pfizer branding and indicates an 18 gauge, 1 1/2 inch needle is included.*

* 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.