Label: SHAO LIN PAIN RELIEF PLASTER- menthol, methyl salicylate plaster
-
Contains inactivated NDC Code(s)
NDC Code(s): 69070-001-05 - Packager: Zhejiang Dingtai 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 October 19, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warning
- Do Not Use
- Ask a Doctor or Pharmacist Before Use If You Are
- When Using This Product
- Stop Use and Ask a Doctor If
- Keep Out of Reach of Children.
-
Directions
Adults and children 12 years of age and older: Apply one or two plasters to affected area once a day. Remove after 12 hours.
Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor.
Children under 2 years of age: Do not use, consult a doctor.
Refer to the above warnings: use otherwise than as directed may be dangerous. - Other Information
-
Inactive Ingredients
PEPPERS, LINDERA AGGREGATA ROOT, BLETILLA STRIATA BULB, ANGELICA DAHURICA ROOT, AMPELOPSIS JAPONICA ROOT, PAWPAW, SPARGANIUM STOLONIFERUM WHOLE, CURCUMA ZEDOARIA LEAF, ANGELICA SINENSIS ROOT, PAEONIA VEITCHII ROOT, CINNAMON, RHEUM PALMATUM WHOLE, FORSYTHIA SUSPENSA WHOLE, DRAGON'S BLOOD, FRANKINCENSE, MYRRH, PANAX NOTOGINSENG ROOT, ACACIA CATECHU WHOLE, BORNEOL
- Questions or Comments?
- Manufacturerd by
- Distributed by
- Drug Facts
-
INGREDIENTS AND APPEARANCE
SHAO LIN PAIN RELIEF PLASTER
menthol, methyl salicylate plasterProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69070-001 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.5 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength PEPPERS (UNII: T5KDM4J239) LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T) BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ) ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) AMPELOPSIS JAPONICA ROOT (UNII: O2672197TF) PAWPAW (UNII: 8P95FP65YO) SPARGANIUM STOLONIFERUM WHOLE (UNII: 873IV8AW3C) CURCUMA ZEDOARIA LEAF (UNII: M9E9LQH7N4) ANGELICA SINENSIS ROOT (UNII: B66F4574UG) PAEONIA VEITCHII ROOT (UNII: VX6GD6M93V) CINNAMON (UNII: 5S29HWU6QB) RHEUM PALMATUM WHOLE (UNII: 75P857ARCY) FORSYTHIA SUSPENSA WHOLE (UNII: RO2K2K561Z) DRAGON'S BLOOD (UNII: M3YJ2C28IC) FRANKINCENSE (UNII: R9XLF1R1WM) MYRRH (UNII: JC71GJ1F3L) PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U) ACACIA CATECHU WHOLE (UNII: TJ6XA84OQF) BORNEOL (UNII: M89NIB437X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69070-001-05 5 in 1 BOX 05/01/2010 1 1 g 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 05/01/2010 Labeler - Zhejiang Dingtai Pharmaceutical Co.; Ltd (420598724) Registrant - Zhejiang Dingtai Pharmaceutical Co.; Ltd (420598724) Establishment Name Address ID/FEI Business Operations Zhejiang Dingtai Pharmaceutical Co.; Ltd 420598724 manufacture(69070-001)