Label: TOTALARTHRITIS- camphor, eugenol, menthol ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 73417-852-52 - Packager: PhytoBiologic Pharmaceutics LLC
- 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 July 24, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- TotalArthritis Active Ingredients
- Purpose
- Uses
- Warnings for external use only
- When using this product
- Stop use of this product and consult a doctor If
- If pregnant or breast-feeding, or symptoms persist, consult medical professional before use
- Keep out of reach of children, if swallowed, get Imrnedlate medical help.
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Directions
- Apply a generous amount of the ointment (~1g) on affected area 3 times daily and massage gently. For faster results, apply
local heat with a heat lamp or heat pad after each application.
- For chronic severe conditions, use the ointment for 6 to 9 months and as advised by the physician*.
* Individual results vary depending on the chronic conditions, age and time length of suffering.
- Other information
- Inactive Ingredients
- Questions or Comments ?
- Principal Display Panel - 25 g Jar Carton NDC 73417-852-52 TotalArthritis TM Net Wt: 0.90 OZ (25g)
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INGREDIENTS AND APPEARANCE
TOTALARTHRITIS
camphor, eugenol, menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73417-852 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 40 mg in 1 g EUGENOL (UNII: 3T8H1794QW) (EUGENOL - UNII:3T8H1794QW) EUGENOL 40 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 40 mg in 1 g Inactive Ingredients Ingredient Name Strength NIGELLA SATIVA SEED (UNII: 4LVZ0Z0ITT) EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW) MUSTARD OIL (UNII: TYY1MA9BSY) PETROLATUM (UNII: 4T6H12BN9U) PEPPERMINT OIL (UNII: AV092KU4JH) AZADIRACHTA INDICA LEAF (UNII: HKY915780T) YELLOW WAX (UNII: 2ZA36H0S2V) RUBIA CORDIFOLIA ROOT (UNII: 4V873H15CG) ALOE VERA LEAF (UNII: ZY81Z83H0X) TURMERIC (UNII: 856YO1Z64F) GINGER (UNII: C5529G5JPQ) Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73417-852-52 1 in 1 CARTON 08/12/2021 1 25 g in 1 JAR; 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 08/12/2021 Labeler - PhytoBiologic Pharmaceutics LLC (117103844) Registrant - PhytoBiologic Pharmaceutics LLC (117103844) Establishment Name Address ID/FEI Business Operations PhytoBiologic Pharmaceutics LLC 117103844 manufacture(73417-852) , label(73417-852)