Allayurveda.Com (Pvt) Ltd

11 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• DIETARYING3 refused lines

  Dietary ingredients not listed

  The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.

• LIST INGRE3 refused lines

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• NEEDS FCE3 refused lines

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• NO ENGLISH3 refused lines

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• NO PROCESS3 refused lines

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

• PLANT PART3 refused lines

  PLANT PART

• UNAPPROVED3 refused lines

  Unapproved new drug

  The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

• POISONOUS2 refused lines

  Poisonous or deleterious substance

  The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

Questions about Allayurveda.Com (Pvt) Ltd

Is Allayurveda.Com (Pvt) Ltd on an FDA import alert?

Yes. As of October 26, 2026, Allayurveda.Com (Pvt) Ltd is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for baidyanath brand agnitundi bati; baidyanath brand shankh bati; baidyanath brand sarivadi bati; baidyanath brand saptamrit lauh; baidyanath brand rajahpravartini bati; baidyanath brand marichyadi bati; baidyanath brand gaisantak bati; baidyanath brand chitrakadi bati; baidyanath brand brahmi bati; b…; FDA published the listing on April 1, 2021.

Has FDA refused shipments from Allayurveda.Com (Pvt) Ltd?

Yes. FDA refused 9 shipment lines from Allayurveda.Com (Pvt) Ltd between September 17, 2019 and July 23, 2026. The most recent, on July 23, 2026, was ashwagandha (herbal & botanicals, not teas), charged as POISONOUS (poisonous or deleterious substance).

Why did FDA refuse Allayurveda.Com (Pvt) Ltd's shipments?

The most frequent charges are DIETARYING (dietary ingredients not listed, 3 lines) and LIST INGRE (ingredients not listed, 3 lines).

When was Allayurveda.Com (Pvt) Ltd last inspected by FDA?

FDA's most recent inspection of Allayurveda.Com (Pvt) Ltd with a final classification is dated October 8, 2021 and was classified NAI (No Action Indicated).

What is Allayurveda.Com (Pvt) Ltd's FEI number?

Allayurveda.Com (Pvt) Ltd's FDA Establishment Identifier (FEI) is 3011280464.

Can shipments from Allayurveda.Com (Pvt) Ltd still enter the U.S.?

Shipments of baidyanath brand agnitundi bati; baidyanath brand shankh bati; baidyanath brand sarivadi bati; baidyanath brand saptamrit lauh; baidyanath brand rajahpravartini bati; baidyanath brand marichyadi bati; baidyanath brand gaisantak bati; baidyanath brand chitrakadi bati; baidyanath brand brahmi bati; b… from Allayurveda.Com (Pvt) Ltd can be detained without physical examination under Import Alert 99-42; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).