VITAMIN A AND D ointment

Vitamin A and D by

Drug Labeling and Warnings

Vitamin A and D by is a Otc medication manufactured, distributed, or labeled by MIDWOOD BRANDS, LLC, Jell pharmaceuticals Pvt. Ltd., Jell Pharmaceuticals Pvt Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Lanolinn - 15.5%

Petrolatum - 53.4%

PURPOSE

Purpose

Skin protectant

INDICATIONS & USAGE

Uses

• helps treat and prevent diaper rash
• temporarily protects minor cuts, scrapes and burns
• temporarily protects and helps relieve chapped, chafed or cracked skin and lips
• protects chafed skin due to diaper rash and helps seal out wetness

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use in eyes

• not for extensive burns or serious cuts, consult a physician

STOP USE

Stop use and ask a doctorif redness, irritation, swelling or pain persists or increases or if infection develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions

• Apply generously and massage until absorbed. Repeat as necessary.

Inactive Ingredients

Cod Liver Oil
Fragrance
Light Mineral Oil

Microcrystalin Wax

Water

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

Vitamin A&D Cream

NET WT 4 OZ (113 g)

INGREDIENTS AND APPEARANCE

VITAMIN A AND D 
vitamin a and d ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55319-603
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	53.4 g  in 100 g
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	15.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
COD LIVER OIL (UNII: BBL281NWFG)
FRAGRANCE 13576 (UNII: 5EM498GW35)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55319-603-01	113 g in 1 TUBE; Type 0: Not a Combination Product	07/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/12/2024

Labeler - MIDWOOD BRANDS, LLC (024472631)

Registrant - Jell pharmaceuticals Pvt. Ltd. (726025211)

Establishment
Name	Address	ID/FEI	Business Operations
Jell Pharmaceuticals Pvt Ltd		726025211	manufacture(55319-603)