ORIGINAL POWER REFIRMING AMPOULE

Product NDC
51346-218
11-digit product format
513460218
Labeler code
51346
Product ID
51346-218_beb8a61f-0223-4fb0-8f58-c82ff481d4dd
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
LIQUID
Route
TOPICAL
Labeler
NATURE REPUBLIC CO., LTD.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-02-01
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
1 mg/30mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-218-012021-07-05C16284748780-19d75b9cf-e4a7-f424-e053-dadaa90a57cef99c2c3b-6b87-4b06-b3e9-9d4f64b87f8e
51346-218-012020-01-31C16284748780-19d75b9cf-e4a7-f424-e053-dadaa90a57cef99c2c3b-6b87-4b06-b3e9-9d4f64b87f8e