Phexx Gel
Product Images NDC 69751-101

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Phexx (NDC 69751-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Evofem, 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

Chemical Structure (Phexx 01)

Chemical Structure (Phexx 01)
Chemical structure of lactic acid, L-, one of the active ingredients in Phexx vaginal gel. The diagram shows the molecular arrangement with hydroxyl and carboxyl functional groups clearly marked.*
FDA Label Image

Chemical Structure (Phexx 02)

Chemical Structure (Phexx 02)
Chemical structure of citric acid monohydrate, showing three carboxyl groups and one hydroxyl group on a central carbon chain.*
FDA Label Image

Chemical Structure (Phexx 03)

Chemical Structure (Phexx 03)
Chemical structure of potassium bitartrate depicted in a 2D skeletal formula showing atoms and bonds, including a potassium ion and carboxyl groups.*
FDA Label Image

Figure A (Phexx 04)

Figure A (Phexx 04)
Illustration showing the parts of a pre-filled applicator for Phexx vaginal gel. Labeled components include the pink cap, pre-filled applicator, grooved area, tip of the plunger rod, and the plunger rod itself.*
FDA Label Image

Figure B (Phexx 05)

Figure B (Phexx 05)
An instructional illustration showing a hand holding and separating two elongated gel sachets or packets by tearing at notched ends. The image suggests how to open the gel packaging for use.*
FDA Label Image

Figure C (Phexx 06)

Figure C (Phexx 06)
An instructional illustration showing how to assemble a syringe applicator device. The steps include removing a cap, pulling back a plunger, and assembling the syringe parts ready for use.*
FDA Label Image

Figure D (Phexx 07)

Figure D (Phexx 07)
An instructional illustration showing a hand removing a protective cap from a vaginal gel applicator prior to use. The other hand holds the gel applicator horizontally with the plunger end visible.*
FDA Label Image

Figure E (Phexx 08)

Figure E (Phexx 08)
An illustration showing a hand holding a vaginal gel applicator, demonstrating how to hold the applicator for use. The applicator has a plunger and a cap on the dispensing end.*
FDA Label Image

Figure F (Phexx 09)

Figure F (Phexx 09)
An instructional illustration showing a hand inserting a vaginal gel applicator into the vaginal canal, demonstrating correct placement technique for the Phexx vaginal gel product.*
FDA Label Image

Figure G (Phexx 10)

Figure G (Phexx 10)
An instructional line drawing showing a hand inserting a vaginal gel applicator into the vaginal canal. An arrow indicates the direction of insertion for proper administration.*
FDA Label Image

Figure H (Phexx 11)

Figure H (Phexx 11)
An instructional illustration showing the insertion of a vaginal gel applicator into the female genital area. A hand is depicted holding the applicator with an arrow indicating the direction of insertion.*
FDA Label Image

Principal Display Panel (12 Applicator Box)

Principal Display Panel (12 Applicator Box)
Phexx vaginal gel packaging label displays the proprietary name Phexx with active ingredients lactic acid, citric acid, and potassium bitartrate in concentrations of 1.8%, 1%, and 0.4%, respectively. The label includes storage instructions, usage directions, and a caution that the product does not protect against HIV or other sexually transmitted diseases. It is manufactured by Evofem, Inc., and each single-dose pre-filled applicator contains 5 g of gel. The label features a distinct pink and orange geometric design.*

* 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.