PROPOLIS SOFTENING TONER

Product NDC

59535-0219

11-digit product format

595350219

Labeler code

59535

Product ID

59535-0219_3b4312e4-d8d1-203c-e054-00144ff88e88

Type

HUMAN OTC DRUG

Nonproprietary name

PROPOLIS WAX

Dosage form

LIQUID

Route

TOPICAL

Labeler

AMI Cosmetic Co.,Ltd.

Marketing category

UNAPPROVED DRUG

Marketing start

2016-08-30

Marketing end

0000-00-00

Substance

PROPOLIS WAX; N

Active strength

1 g/100mL; g/100m

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record