7TH MANNA PAIN RELIEF DROPS (menthol, camphor- synthetic liquid

7th MANNA PAIN RELIEF DROPS by

Drug Labeling and Warnings

7th MANNA PAIN RELIEF DROPS by is a Otc medication manufactured, distributed, or labeled by 7TH MANNA (USA) PTE. LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Menthol 10%

Camphor 3%

Purpose

Topical Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:

• arthritis
• sprains
• strains
• bruises
• simple backaches

Warnings

For external use only.

Use only as directed.

Flammable

• keep away from fire, flame, sparks and heated surfaces
• tighten cap firmly

When using this product

• avoid contact with the eyes
• do not apply to wounds or damaged skin
• do not bandage tightly

Stop use and ask a doctor if

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

If pregnant or breast-feeding,

ask a healthcare provider before use.

Keep out of reach of children.

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

Directions

For adults: Apply to affected area no more than 3 to 4 times daily

Other Information

• Store at room temperature
• Do not use if printed safety seal on cap is broken or missing

Inactive Ingredients

Aloe Barbadensis Leaf (Aloe vera gel) Juice, Aqua (Deionized water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Emu Oil, Dimethyl Sulfoxide (DMSO),Ethylhexylglycerin, HypericumPerforatum (St.John's Wort),Isopropyl Alcohol, Methyl Salicylate (Wintergreen) Oil, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B.

Questions?

Call us at 1-800-230-8055

Package Labeling:

INGREDIENTS AND APPEARANCE

7TH MANNA PAIN RELIEF DROPS 
menthol, camphor (synthetic) liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71856-423
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GREEN OLIVE (UNII: 6HD2W46UEG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
EMU OIL (UNII: 344821WD61)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYL SALICYLATE (UNII: LAV5U5022Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71856-423-00	1 in 1 BOX	09/25/2023
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017B	09/25/2023

Labeler - 7TH MANNA (USA) PTE. LTD. (659264720)