FRANKINCENSE AND MYRRH NERVE COMBO PACK- menthol kit

Frankincense and Myrrh Nerve Combo Pack by

Drug Labeling and Warnings

Frankincense and Myrrh Nerve Combo Pack by is a Otc medication manufactured, distributed, or labeled by Wise Consumer Products, Innovation Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

42346-550-86

Active ingredient

Menthol 1.3%

Purpose

Menthol 1.3%......................Topical Analgesic

Uses

For the temporary relief of minor aches and pains.

Warnings

For external use only

When using this product

• avoid contact with the eyes
• do not bandage tightly

Do not use

• on wounds or damaged skin
• over large areas of the body

Stop use and ask a doctor if

• condition worsens
• irritation occurs
• symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding, ask a health professional before use.

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.

Children under 12 years of age: consult a doctor.

Other information

• store in a cool, dry place
• tamper resistant: do not use if seal undertube cap is broken or missing

Inactive ingredients

Bergamot Oil, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetyl Alcohol, Cinnamon Oil, Cocoa Butter, Coconut Oil, Eucalyptus Oil, Frankincense Oil, Geranium Oil, Glycerin, Glyceryl Stearate, Lanolin, Lemon Oil, Methylparaben, Myrrh Oil, Nutmeg Oil, Palmitic Acid, Polysorbate 60, Propylparaben, Rosemary Oil, Shea Butter, Sodium Hydroxide, Stearic Acid, Water, Xanthan Gum

Questions or comments?

1-877-917-9674 Monday – Friday, 9 a.m.–5 p.m. ESTor visit www.frankincensemyrrh.com

42346-360-59

Active ingredient

Menthol 2%

Purpose

Menthol 2%......................Topical Analgesic

Uses

For temporary relief of minor aches and pains

Warnings

For external use only

Do not use

• on wounds or damaged skin
• over large areas of the body

When using this product

• avoid contact with the eyes
• do not bandage tightly

Stop use and ask a doctor if

• condition worsens
• irritation occurs
• symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reacho f children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Adults and children 12 years of age and older:
• apply 10-30 drops into hand and massage into affected areas
• can be used up to 4 times daily
• children under 12 years of age: consult a doctor

Other information

• store in a cool, dry place
• tamper resistant: do not use if seal around bottle neck is broken or missing
• keep carton, it contains important information

Inactive ingredients

Bergamot Oil, Cinnamon Oil, Eucalyptus Oil, Frankincense Oil, Geranium Oil, Lemon Oil, Myrrh Oil, Nutmeg Oil, Rosemary Oil, Sunflower Oil, Tocopheryl Acetate

Questions or comments?

1-877-917-9674

M-F, 9am-5pm EST or www.frankincensemyrrh.com

PRINCIPAL DISPLAY PANEL

Frankincense & Myrrh

Combo Pack

Deep Penetrating Relief

Menthol 2%

2 fl oz (59mL)

Menthol 1.3%

3 fl oz (85g)

INGREDIENTS AND APPEARANCE

FRANKINCENSE AND MYRRH NERVE COMBO PACK 
menthol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42346-378

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42346-378-65	1 in 1 KIT; Type 0: Not a Combination Product	12/29/2025

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE, DROPPER	59 mL
Part 2	1 TUBE	85 g

Part 1 of 2

SOOTHING NERVE RELIEF 
menthol oil

Product Information
Item Code (Source)	NDC: 42346-360
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CINNAMON OIL (UNII: E5GY4I6YCZ)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
NUTMEG OIL (UNII: Z1CLM48948)
LEMON OIL (UNII: I9GRO824LL)
BERGAMOT OIL (UNII: 39W1PKE3JI)
FRANKINCENSE OIL (UNII: 67ZYA5T02K)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ROSEMARY OIL (UNII: 8LGU7VM393)
MYRRH OIL (UNII: H74221J5J4)
SUNFLOWER OIL (UNII: 3W1JG795YI)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42346-360-59	1 in 1 CARTON
1		59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/29/2025

Part 2 of 2

SOOTHING NERVE THERAPY 
menthol lotion

Product Information
Item Code (Source)	NDC: 42346-550
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
EUCALYPTUS OIL (UNII: 2R04ONI662)
WATER (UNII: 059QF0KO0R)
MYRRH OIL (UNII: H74221J5J4)
COCOA BUTTER (UNII: 512OYT1CRR)
LANOLIN (UNII: 7EV65EAW6H)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
METHYLPARABEN (UNII: A2I8C7HI9T)
SHEA BUTTER (UNII: K49155WL9Y)
LEMON OIL (UNII: I9GRO824LL)
STEARIC ACID (UNII: 4ELV7Z65AP)
GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
COCONUT OIL (UNII: Q9L0O73W7L)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
BERGAMOT OIL (UNII: 39W1PKE3JI)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 60 (UNII: CAL22UVI4M)
CETYL ALCOHOL (UNII: 936JST6JCN)
ROSEMARY OIL (UNII: 8LGU7VM393)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FRANKINCENSE OIL (UNII: 67ZYA5T02K)
NUTMEG OIL (UNII: Z1CLM48948)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CINNAMON OIL (UNII: E5GY4I6YCZ)
PALMITIC ACID (UNII: 2V16EO95H1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42346-550-86	1 in 1 CARTON
1		85 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/29/2025

Labeler - Wise Consumer Products (006459643)

Establishment
Name	Address	ID/FEI	Business Operations
Innovation Labs, Inc.		117109069	manufacture(42346-378, 42346-360, 42346-550)