Label: TENDINITICA SYNERGY FOR TREATMENT OF TENDINITIS- tendinitica oil
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Contains inactivated NDC Code(s)
NDC Code(s): 70470-1139-5 - Packager: PHYTOPIA 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 April 2, 2016
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- ACTIVE INGREDIENT
- PURPOSE
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
- WARNINGS
- PainAway-With natural Peppermint and Balsam Peru Oil
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INGREDIENTS AND APPEARANCE
TENDINITICA SYNERGY FOR TREATMENT OF TENDINITIS
tendinitica oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70470-1139 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.3 mg in 50 mg Inactive Ingredients Ingredient Name Strength MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) CLARY SAGE OIL (UNII: 87L0D4U3M0) LAVENDER OIL (UNII: ZBP1YXW0H8) OLIVE OIL (UNII: 6UYK2W1W1E) SUNFLOWER OIL (UNII: 3W1JG795YI) JOJOBA OIL (UNII: 724GKU717M) ROSEMARY OIL (UNII: 8LGU7VM393) BERGAMOT OIL (UNII: 39W1PKE3JI) Product Characteristics Color brown (50ml per bottle) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70470-1139-5 500 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 04/01/2016 Labeler - PHYTOPIA CO., LTD. (656940504) Registrant - PHYTOPIA CO., LTD. (656940504) Establishment Name Address ID/FEI Business Operations Phytopia Co., Ltd. 656940504 manufacture(70470-1139)