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Vitamin A and D by Universal Distribution Center LLC

Medically reviewed on August 4, 2016

Dosage form: cream
Ingredients: VITAMIN A 181.8[iU] in 1g, VITAMIN D 1200[iU] in 1g
Labeler: Universal Distribution Center LLC
NDC Code: 52000-026

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Vitamin A&D Cream

Active Ingredients

Vitamin A  181.8 IU

Vitamin D   1200 IU

Purpose

Skin protectant

Uses

  • helps prevent diaper rash
  • heals dry, flaky and chafed skin
  • soothes and protects minor cuts and burns

Warnings

For external use only

Do not use in eyes

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

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

Keep out of reach of children.

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

Directions

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

Other information

  • Store at controlled room temperature 15ºC to 30ºC (59ºF to 86ºF). Lot No. & Exp.Date see crimp of tube.

Inactive ingredients

Cetyl Alcohol, DMDM Hydantoin, Glyceryl Monostearate, Methylparaben, Mineral Oil, Polysorbate 20, Propylparaben, Stearic Acid,  Trisodium EDTA, and Water.

PRINCIPAL DISPLAY PANEL

Vitamin A&D Cream

NET WT 1 OZ (28 g)

VITAMIN A AND D 
vitamin a and d cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-026
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VITAMIN A (VITAMIN A) VITAMIN A181.8 [iU]  in 1 g
VITAMIN D (CHOLECALCIFEROL) VITAMIN D1200 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL 
DMDM HYDANTOIN 
GLYCERYL MONOSTEARATE 
METHYLPARABEN 
MINERAL OIL 
POLYSORBATE 20 
PROPYLPARABEN 
STEARIC ACID 
EDETATE TRISODIUM 
WATER 
Packaging
#Item CodePackage Description
1NDC:52000-026-371 TUBE in 1 CARTON
1NDC:52000-026-3928 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34708/04/2016
Labeler - Universal Distribution Center LLC (019180459)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
NameAddressID/FEIOperations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-026)

 
Universal Distribution Center LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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