NUTURNA ARTHRITIS INTENSIVE CONCENTRATE FOR PAIN RELIEF AND RECOVERY- menthol cream 
Nuturna International LLC

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NUTURNA (as PLD) - Arthritis Intensive Concentrate for Pain Relief & Recovery (81996-244)

Drug Facts

Active Ingredients

Menthol 3.70%

Purpose

Topical Analgesic

Uses:

Warnings:

For external use only

Do not use

  • On damaged or broken skin.

When using this product

  • Avoid contact with the eyes. 
  • Do not bandage tightly

Stop use and ask a doctor if

  • Rash or irritation develops and lasts.
  • Condition worsens, or if symptoms persist for more than 7 days or clear up and occurs again within a few days.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding,

ask a health professional before use.

Directions:

Inactive ingredients:

Aloe Barbadensis Leaf(Aloe Vera Gel)Juice, Arnica Montana Flower Extract, Carbomer, Ilex Paraguariensis (Yerba Mate) Extract, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Oil, Methylisothiazolinone, Methylsulfonylmethane (MSM), Polysorbate-20, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD & C Blue # 1.

Other information:

Questions ?

customerservice@nuturna.com

Package Labeling:57g

Label

Package Labeling:114g

Label2

Package Labeling:228g

Label3

NUTURNA ARTHRITIS INTENSIVE CONCENTRATE FOR PAIN RELIEF AND RECOVERY 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81996-244
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3.7 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
TEA TREE OIL (UNII: VIF565UC2G)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TROLAMINE (UNII: 9O3K93S3TK)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81996-244-0257 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
2NDC:81996-244-04114 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
3NDC:81996-244-08228 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/22/2020
Labeler - Nuturna International LLC (117795246)

Revised: 1/2024
Document Id: 0894ba40-2d73-f381-e063-6394a90a2b21
Set id: 46384348-d48c-485c-aaf0-75a0a688ca85
Version: 6
Effective Time: 20240104
 
Nuturna International LLC