PHARMACYS PRESCRIPTION VAPOR RUB

Product NDC
76176-112
11-digit product format
761760112
Labeler code
76176
Product ID
76176-112_76ac3da9-a44d-265c-e053-2a91aa0a9752
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
GEL
Route
TOPICAL
Labeler
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2018-08-01
Marketing end
0000-00-00
Substance
MENTHOL; EUCALYPTUS OIL; CAMPHOR (NATURAL)
Active strength
1 g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76176-112-0176176011201110 g in 1 JAR (76176-112-01) 110 g2018-08-010000-00-00NoNoCurrent