Other

Warning Letter — AAL Trading Inc.

Warning Letter — Eherbs Imports, Inc

Warning Letter — Delight Distribution Inc.

Warning Letter — Piquin Y Sabores Distributors LLC

Warning Letter — Prida Import & Export LLC

Warning Letter — Beauty Store LLC

Warning Letter — Mineral BioSciences, LLC

Warning Letter — AF Import & Wholesale Co

Warning Letter — Diamond Distributions LLC

Warning Letter — Pure Arylcyclohexylamine Store / www.arylcyclohexylamine.com

Warning Letter — Wild Arabic Herbs

Warning Letter — Telos Trading Limited dba Alwinshop

Warning Letter — Great Enterprise - Group - Inc.

Warning Letter — Ezra Holdco LLC dba Ezra

Total Nutrition Inc. Expands Recall of TNVitamins and Doctor’s Pride Ultra Potent Complete Green Superfood Moringa Capsules Because of Possible Health Risk Following Further Supply Chain Review

FDA Expands Sunscreen Options for the First Time in 20 Years

Warning Letter — Jose M. Carpio, M.D.

Warning Letter — Revlon Group Holdings, LLC

Warning Letter — Erkul Kozmetik Sanayi ve Ticaret A.S.

GO Raw LLC. Expands Voluntary Recall to Include One Lot of Steve’s Real Food Freeze-Dried Chicken Recipe Due to Low Thiamine (Vitamin B1) Levels

Target Recalls Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes Due to Potential Microbial Contamination

Total Nutrition Inc. Expands Recall of TNVitamins and Doctor’s Pride Ultra Potent Complete Green Superfood Moringa Capsules Because of Possible Health Risk

Better Weather Actives LLC Recalls Better Weather Fix Elixir Due to Undeclared Mitragynine and Mitragynine Pseudoindoxyl

Total Nutrition Inc. Recalls TNVitamins and Doctor’s Pride Ultra Potent Complete Green Superfood Moringa Capsules Because of Possible Health Risk

Warning Letter — Zap Expo Center Inc.

Mogo Moringa LLC Announces Voluntary Recall of Select Lots of Moringa Capsules Due to Possible Salmonella Contamination

JXK Enterprises, Inc Issues Voluntary Nationwide Recall of Boner Bears Chocolate Due to Undeclared Sildenafil

Warning Letter — Great One Trading Inc.

Warning Letter — JW Nutritional LLC

Warning Letter — Sahara Enterprise Inc.

Warning Letter — JMT Inter LLC

FDA Advances Drug Repurposing to Address Unmet Medical Needs

Best Supplements Best Prices Issues Voluntary Nationwide Recall of WAP Sensual Enhancement Capsules Due to Presence of Undeclared Sildenafil, Tadalafil, and Flibanserin

XD Investments LLC Recalls Better Weather Fix Elixir Products Due to Undeclared Mitragynine and Mitragynine Pseuoindoxyl

FDA Expands AI Capabilities and Completes Data Platform Consolidation

FDA Launches One-Day Inspectional Assessments to Strengthen and Expand Oversight

Albright’s Raw Pet Food Announces Voluntary Recall of Select Chicken Recipe for Dogs Complete and Balanced, 1 lb Bricks (Lot #C001730)

Warning Letter — Ray’s Vitamins

Warning Letter — Active Cosmetics Manufacturing Inc.

FDA Proposes to Exclude Semaglutide, Tirzepatide, and Liraglutide on 503B Bulks List

FDA Announces Major Steps to Implement Real-Time Clinical Trials

Warning Letter — The Wilatta Group Inc.: Office of Inspections and Investigations

FDA Accelerates Action on Treatments for Serious Mental Illness Following Executive Order

FDA Achieves Year 1 Goals in Reducing Animal Testing in Drug Development

Revival Animal Health, LLC Voluntarily Recalls Canine Milk Replacers Due to Elevated Levels of Vitamin D

FDA Takes Step Forward on Testosterone Therapy for Men

FDA Reminds More Than 2,200 Sponsors and Researchers to Disclose Trial Results

Blueroot Health Expands Voluntary Allergy Alert on Undeclared Egg, Hazelnut, and Soy in Vital Nutrients Aller-C Dietary Supplements

Blaine Labs, Inc Issues Voluntary Nationwide Recall of Wound Care Gel Products Due to Microbial Contamination

Nalpac Issues Voluntary Nationwide Recall of DTF Sexual Chocolate Due to the Presence of the Pharmaceutical Ingredient’s Sildenafil and Tadalafil

Aphreseller (Buy-herbal.com) Issues Voluntary Nationwide Recall of Kian Pee Wan Capsules Due the Presence of Undeclared Dexamethasone and Cyproheptadine

FDA Schedules Public Meeting on the Commissioner’s National Priority Voucher Pilot Program

FDA Launches New Adverse Event Look-Up Tool