Vitamin C and E Ferulic Glow Potion by Novamed Healthcare Private Limited

Vitamin C and E Ferulic Glow Potion by

Drug Labeling and Warnings

Vitamin C and E Ferulic Glow Potion by is a Otc medication manufactured, distributed, or labeled by Novamed Healthcare Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VITAMIN C AND E FERULIC GLOW POTION- vitamin c, vitamin e, ferulic acid liquid 
Novamed Healthcare Private Limited

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Dosage and Administration

Apply 2-3 drops of serum on clean, dry skin, gently patting it for absorption. For optimal results, use in the morming (AM) with SPF and in evening (PM) a part of your daily skin care regimen. Suitable for skin types

Indications and Usage

Uses:

• Reduces Hyperpigmentation
• Improves Skin Tone
• Hydrates Skin
• Anti-aging Properties
• Strengthens Skin Barrier
• Promotes Collagen Production
• Accelerates Cell Regeneration

Inactive Ingredients

• Polysorbate 20
• Phenoxyethanol
• Sodium Hydroxide
• EDTA
• Water

Active Ingredients

• 3-0 Ethyl Ascorbic Acid
• Ferulic Acid
• Alpha Arbutin
• Licorice
• Alpha Tocopherol Acetate
• Sodium Hyaluronate
• Panthenol

Keep out of the reach of children

Keep out of the reach of children

Purpose

Ingredient Purpose

3-O Ethyl Ascorbic Acid Skin Lightening

Ferulic Acid Prevents discoloration

Alpha Arbutin Skin Lighteneing + Sun screen

Licorice Skin Lighteneing

Alpha Tocopherol Acetate Anti oxidant

Sodium Hyaluronate Moisturizing agent

Panthenol Moisturizing +skin repairing+anti-Inflammatory Agent

Warnings

• Avoid usage alongside Retinoids, AHAs / BHAs and Benzyol Peroxide
• For external use only
• Avoid disrect contact with eyes
• Perform a patch test before initial use, if irritation occurs, discontinue use and consult a dermatologist
• Store in a cool dry place

VITAMIN C AND E FERULIC GLOW POTION 
vitamin c, vitamin e, ferulic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84859-113
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM HYALURONATE (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY)	SODIUM HYALURONATE	200 mg  in 30 mL
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	600 mg  in 30 mL
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) (3-O-ETHYL ASCORBIC ACID - UNII:6MW60CB71P)	3-O-ETHYL ASCORBIC ACID	3000 mg  in 30 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL ACETATE	600 mg  in 30 mL
ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5)	ALPHA-ARBUTIN	600 mg  in 30 mL
LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883)	LICORICE	0.6 mg  in 30 mL
FERULIC ACID (UNII: AVM951ZWST) (FERULIC ACID - UNII:AVM951ZWST)	FERULIC ACID	150 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.3 mL  in 30 mL
EDTA (UNII: 9G34HU7RV0)	60 mg  in 30 mL
POLYSORBATE 20 (UNII: 7T1F30V5YH)	450 mg  in 30 mL
WATER (UNII: 059QF0KO0R)	30 mL  in 30 mL
SODIUM HYDROXIDE (UNII: 55X04QC32I)	0.3 mg  in 30 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84859-113-01	1 in 1 BOX	01/20/2025	04/24/2025
1	NDC: 84859-113-30	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	M016	01/20/2025	04/24/2025

Labeler - Novamed Healthcare Private Limited (645814547)

Registrant - Novamed Healthcare Private Limited (645814547)

Establishment
Name	Address	ID/FEI	Business Operations
Novamed Healthcare Private Limited		645814547	manufacture(84859-113) , label(84859-113) , pack(84859-113)

Revised: 5/2025

Document Id: 3528c368-7a8d-ad18-e063-6394a90ab065

34390-5

Set id: 2c1f9be4-9785-2377-e063-6294a90ae7f4

Version: 2

Effective Time: 20250515