Sprintec Kit
Product Images NDC 63187-911
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Sprintec (NDC 63187-911). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Proficient Rx Lp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Ethinyl Estradiol Structural Formula (Image 02)
Ethiny! Estradiol is likely an incomplete text as it appears to be a combination of two different words: ethinyl and estradiol. Ethinyl estradiol is a type of estrogen hormone used in combination with progestin as a form of hormonal birth control. Estradiol is a female sex hormone usually used in hormone replacement therapy for menopausal women. However, without further context or information, it is difficult to determine the intended meaning or purpose of this text.*
Fewer-more Pregnancies Image (Image 03)
This text is a list of different birth control methods, including options such as implants, injections, intrauterine devices, sterilization, birth control pills, skin patches, vaginal rings, condoms, diaphragms, and natural methods such as avoiding intercourse during fertile days or using spermicide and withdrawal.*
Blister Image (Image 04)
Blister Image (Image 05)
This is a prescription drug with the generic name norgestimate and ethinyl estradiol. The drug is marketed in the form of tablets with a strength of 0.250 mg/0.035 mg and is known by the brand name Sprintec. There is a specific storage instruction to keep the tablets at a temperature between 20°C to 25°C. The text also mentions a distributor named Aue Bunyes located at 1049 S AIOFO.*
63187-911-28 (Image 06)
This is a label information of a pharmaceutical product named Sprintec 0.25mg/0.035mg, which comes in a package of 1x28 28 Day Tablets. The NDC number of the product is 63187-911-28, and it has been relabeled by ProficientRx LP, located in Thousand Oaks, CA 91320. The medicine is indicated for prescription-only use. The product is manufactured by Teva Pharmaceuticals USA, INC. The label includes details about lot number, expiration date (Exp.), and storage conditions. In case of any queries, the label suggests referring to the package insert.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.