Label: WU YANG BRAND MEDICATED- menthol, methyl salicylate plaster
-
Contains inactivated NDC Code(s)
NDC Code(s): 61822-0045-1, 61822-0045-2 - Packager: GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 13, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WU YANG BRAND MEDICATED
menthol, methyl salicylate plasterProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61822-0045 Route of Administration TOPICAL, TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 6 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 g Inactive Ingredients Ingredient Name Strength BLACK CATECHU (UNII: 55J167EEON) POLYGONUM CUSPIDATUM WHOLE (UNII: 1VDG5Y5HS6) TARAXACUM MONGOLICUM (UNII: 4E8QL88U6H) DAEMONOROPS DRACO RESIN (UNII: 787Z7N9UCU) DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q) MAMMAL BONE, FOSSILIZED (UNII: 0N1T3913DA) GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) SAFFLOWER (UNII: 4VBL71TY4Y) DIPSACUS ASPER ROOT (UNII: LB1GQP4253) MYRRH (UNII: JC71GJ1F3L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61822-0045-1 10 in 1 BOX; Type 0: Not a Combination Product 10/19/2001 2 NDC:61822-0045-2 1 in 1 CAN; Type 0: Not a Combination Product 10/19/2001 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/19/2001 Labeler - GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY (530854970) Establishment Name Address ID/FEI Business Operations GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO., LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY 530854970 manufacture(61822-0045)