Dr Blue Pain Relieving Gel — Class III drug recall D-1149-2015
Terminated recall by Indiana Botanic Gardens, Inc, reported 2015-07-01, distributed nationwide. Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ing
| Recall number | D-1149-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Indiana Botanic Gardens, Inc, Hobart, IN, United States |
| Recall initiated | 2015-06-04 |
| Classified | 2015-06-25 |
| Reported by FDA | 2015-07-01 |
| Terminated | 2016-03-21 |
| Distributed | Nationwide (US) |
| Reason classes | potency |
| NDC | 10578-0035-04, 10578-0035-05 |
| Lot numbers | 10/16, 6086221 |
Product
Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains of muscles and joints, a) 2 oz. Tube, NDC 10578-035-05, b) 5 oz. Jar, NDC 10578-035-04, Manufactured by Indiana Botanic Gardens, Hobart, IN 46342
Reason for recall
Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ingredient menthol.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1149-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.