Label: SHENNONG ANALGESIC PLASTER- camphor, menthol, methyl salicylate plaster
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Contains inactivated NDC Code(s)
NDC Code(s): 68048-922-08 - Packager: Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd
- 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 March 16, 2016
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
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Stop use and ask a doctor if
Condition worsens.
Symptoms persist for more than 7 days.
Symptoms clear up and occur again within a few days.
Excessive irritation of the skin develops.
Nausea, vomiting, abdominal discomfort, diarrhea or skin rash occurs.
When using for pain of arthritis: pain persists for more than 10 days and if redness is present.
- Keep out of reach of children.
- Directions
- Other Information
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Inactive Ingredients
PANAX PSEUDOGINSENG ROOT, ANGELICA DAHURICA ROOT, CIBOTIUM BAROMETZ ROOT, NOTOPTERYGIUM INCISUM ROOT, SAPOSHNIKOVIA DIVARICATA ROOT, ACTAEA CIMICIFUGA ROOT, SAFFLOWER, LIGUSTICUM WALLICHII ROOT, ANGELICA SINENSIS ROOT, MYRRH, PARIS POLYPHYLLA WHOLE, FRANKINCENSE, BASIL OIL, ATROPA BELLADONNA, NATURAL LATEX RUBBER, ROSIN, ZINC OXIDE, PETROLATUM, LANOLIN
- Drug Facts
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INGREDIENTS AND APPEARANCE
SHENNONG ANALGESIC PLASTER
camphor, menthol, methyl salicylate plasterProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68048-922 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 4.28 mg in 100 mg MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2.84 mg in 100 mg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 1.4 mg in 100 mg Inactive Ingredients Ingredient Name Strength PANAX PSEUDOGINSENG ROOT (UNII: NMK0ZS613U) ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) CIBOTIUM BAROMETZ ROOT (UNII: 2YP9JGT10R) NOTOPTERYGIUM INCISUM ROOT (UNII: 5Z2WW4J6RI) SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD) ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT) SAFFLOWER (UNII: 4VBL71TY4Y) LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS) ANGELICA SINENSIS ROOT (UNII: B66F4574UG) MYRRH (UNII: JC71GJ1F3L) PARIS POLYPHYLLA WHOLE (UNII: 1E5W175DRX) FRANKINCENSE (UNII: R9XLF1R1WM) BASIL OIL (UNII: Z129UMU8LE) ATROPA BELLADONNA (UNII: WQZ3G9PF0H) NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN) ROSIN (UNII: 88S87KL877) ZINC OXIDE (UNII: SOI2LOH54Z) PETROLATUM (UNII: 4T6H12BN9U) LANOLIN (UNII: 7EV65EAW6H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68048-922-08 8 in 1 BOX 1 2.5 mg in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 06/01/2016 Labeler - Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd (654041649) Registrant - Guangdong Zhanjiang Jimin Pharmaceutical Co, Ltd (654041649) Establishment Name Address ID/FEI Business Operations Guangdong Zhangjiang Jimin Pharmaceutical Co. Ltd 654041649 manufacture(68048-922)