MINERAL OIL- mineral oil liquid 
ATLANTIC BIOLOGICALS CORP.

----------

Mineral Oil USP
831.000/831AA

Distributed by: McKesson Corp. Via Strategic Services LLC.

Memphis, TN 38141 

Money Back Guarantee

www.fosterandthrive.com

Active ingredient

Mineral oil 99.9% 

Purpose

Lubricant laxative

Use

for relief of occasional constipation (irregularity). Generally produces bowel movement in 6 to 8 hours.

Warnings

Do not use 

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

When using this product

do not take with meals. Take only at bedtime.

Stop use and ask a doctor if

you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition.

If breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years of age and over - 1 to 3 Tablespoons (15 to 45 mL) maximum 3 Tablespoons (45 mL) in 24 hours

children 6 to under 12 years of age - 1 to 3 teaspoons (5 to 15 mL) maximum 3 teaspoons (15 mL) in 24 hours

children under 6 years of age - do not use, consult a doctor

Other Information

keep tightly closed. Protect from sunlight.

Inactive ingredients

mixed tocopherols (added as a stabilizer)

(c) 2023 McKesson Corporaation

You may report serious side effects to 833-358-6431

Monday to Friday 9:00am to 7:00pm EST

Principal Display Panel

NDC 17856-1110-01

image 1

MINERAL OIL 
mineral oil liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17856-1110(NDC:70677-1110)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL999 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17856-1110-150 in 1 BOX, UNIT-DOSE02/05/2024
1NDC:17856-1110-230 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM04/17/2023
Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)
Establishment
NameAddressID/FEIBusiness Operations
UNIT DOSE SOLUTIONS360804194repack(17856-1110)

Revised: 2/2024
Document Id: fedc7c39-1abe-420f-99d1-b7fa49873201
Set id: 960502ae-2468-406e-8799-cacb01f2727e
Version: 1
Effective Time: 20240205
 
ATLANTIC BIOLOGICALS CORP.